Reaction mixtures for forming cDNA from an RNA template

ABSTRACT

This invention relates to a process for synthesis of a cDNA in a sample, in an enzymatic reaction, whereby the process comprises the steps: simultaneous preparation of a first enzyme with polyadenylation activity, a second enzyme with reverse transcriptase activity, a buffer, at least one ribonucleotide, at least one deoxyribonucleotide, an anchor oligonucleotide; addition of a sample that comprises a ribonucleic acid; and incubation of the agents of the previous steps in one or more temperature steps, which are selected such that the first enzyme and the second enzyme show activity. The invention further relates to a reaction mixture that comprises a first enzyme with polyadenylation activity, a second enzyme with reverse transcriptase activity, optionally a buffer, optionally at least one ribonucleotide, optionally at least one deoxyribonucleotide, and optionally an anchor oligonucleotide. Moreover, the invention relates to a kit that comprises a corresponding reaction mixture.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of U.S. application Ser. No. 12/377,457, filed Feb., 13, 2009, which issued as U.S. Pat. No. 9,217,173 on Dec. 22, 2015, which is a U.S. National Phase entry of PCT/EP2007/058369, filed Aug. 13, 2007, which claims priority to German Patent Application No. 10 2006 038 113.0, filed Aug. 14, 2006, the disclosures of each of which are incorporated by reference herein in their entireties.

The instant application contains a Sequence Listing which has been submitted via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Mar. 30, 2012, is named 051612US1.txt and is 10,991 bytes in size.

BACKGROUND OF THE INVENTION

The invention relates to the field of molecular biology as well as the research in this field but also the human as well as non-human diagnosis.

The analysis of non-polyadenylated RNA molecules, such as, for example, bacterial RNAs or small RNAs, such as the so-called microRNAs (miRNAs), is made with difficulty and requires special processes. A possible process was recently described in the literature. This process comprises several enzymatic steps that are connected in succession, i.e., first a “tailing” of the RNA with poly-(A)-polymerase and a suitable substrate, typically ATP, is performed. Then, the poly-(A)-reaction is stopped, and the reaction product is purified. Then, the generated poly-(A)-RNA is added in a reverse transcriptase reaction and is converted with suitable primers into cDNA.

TECHNICAL FIELD

The performance of these two enzymatic reactions that are connected in succession is expensive in the implementation and has a number of error sources, for example input of nucleases, loss of material or pipetting errors.

microRNAs (miRNAs) vary in size from about 20 to 25 nucleotides and represent a new family of non-coding RNAs.

They are processed via a so-called “Hairpin Precursor” and can play a role as negative regulators in the gene expression. They thus adjust a number of genes downward (Ambros, V., 2001, MicroRNA's: Tiny Regulators with Great Potential, Cell 107, 823-826). miRNAs are first transcribed as long, “primary transcripts” (they are also referred to as primary miRNAs) (Lee, Y., Jeon, K. et al., 2002, MicroRNA Maturation: Stepwise Processing Subcellular Localisation, Embo J. 21, 4663-4670). These “primary transcripts” are then shortened, whereby the length resulting therefrom is in about 70 nucleotides. So-called “stem-loop structures” are produced; they are also referred to as “pre-miRNAs.” Pre-miRNAs are exported in the cytoplasm. The exporting enzyme is named Exportin-5. They are further processed here, and in this way, an approximately 22-nucleotide-long, mature miRNA molecule is produced (Lee, Y., et al., 2003, The Nuclear RNA's III Drosha Initiates microRNA Processing, Nature 425, 415-419). The most recent studies have proposed that miRNAs play an important role in the development and differentiation. In principle, microRNAs can have a regulating action in two different ways. In plants, miRNAs complement with their corresponding mRNAs by exact complementarity. This leads to a destruction of the target-mRNA by a mechanism that comprises RNA interference (RNAi). In animals, miRNAs prevent gene expression by a mechanism, which comprises Lin-4 and Let-7. Here, the miRNAs are not exactly complementary to their corresponding mRNAs, but they prevent the synthesis and function of the proteins (Ambros, V., 2004, The Functions of Animal microRNAs, Nature, 431, 350-355). Because of the decisive role that the only recently discovered miRNAs play, their detection or analysis is of decisive importance.

In eukaryotes, the synthesis of the 18s, 5.8s and 25/28s rRNAs comprises the processing in modifications of so-called precursor-rRNAs (pre-rRNA) in the nucleolus. This complex course of the rRNA biogenesis comprises many small so-called “small nucleolar RNAs” (snoRNA), which accumulate in the nucleolus. They do this in the form of so-called small nucleolar ribonucleo protein particles (snoRNPs) (Maxwell, E. S. et al., 1995, The Small Nucleolar RNAs, Annual Review Biochem, 35, 897-934).

All snoRNAs that are characterized to date, with the exception of the RNase MRP, fall into two families. The latter are the box c/D and box h/ACA slow RNAs, which can be distinguished by sequence motifs common thereto (Ballakin, A. D. et al., 1996, The RNA World of the Nucleolus: Two Major Families of Small Nucleolar RNAs Defined by Different Box Elements with Related Functions, Cell, 86, 823-834). The genomic organization of the snoRNA genes has a large diversity in various eukaryotes.

In vertebrates, most snoRNAs are introduced within Intrans via “host genes.” Exceptions such as U3 are independently transcribed. In yeast, there are snoRNAs that are introduced into Intrans, but the majority of the snoRNAs are transcribed as single genes with a separate promoter. Clustered snoRNA genes are transcribed upstream by common promoters. Based on the small sizes and the deficient polyadenylation, the detection or the analysis of snoRNAs is a molecular-biological challenge.

The PCR is a frequently-used instrument for the study of microbial organisms and is also used, i.a., to analyze 16S rRNA genes. However, the discovery of new genes in microbial samples is limited by the only conditionally possible synthesis of primers.

Thus, primers are derived for 16S RNA genes from those sequences that are already known from cultivated microbes (Olson, D. J., 1986, Microbial Ecology and Evolution:

A Ribosomal RNA Approach, Annu. Rev. Microbial. 40: 337-365). Based on the systematics that there is recourse to sequences that are already known namely for the extraction of 16S rRNA genes from organisms that are unknown to date, it is probable that the microbial diversity is greatly underestimated and also not isolated.

Just as the 16S rRNA molecules can only be isolated with difficulty, prokaryotic mRNA molecules can be isolated with difficulty owing to a lack of knowledge of the sequence and in particular owing to a lack of poly-A-tail.

The prior art knows a 2-stage process. In this process, an RNA molecule is reacted with the aid of the enzyme poly-A-polymerase and the substrate adenosine triphosphate, such that a polyadenylated ribonucleic acid molecule is produced. This thus polyadenylated ribonucleic acid molecule is purified in an additional step before a reverse transcription takes place in a third step. Reverse transcription is appropriated in the polyadenylated tail, whereby a homopolymer oligonucleotide in general attaches a poly-oligonucleotide to the polyadenylated RNA tail in a complementary manner. The 3′-end of the poly-T-oligonucleotide is now used by the polymerase to produce a deoxyribonucleic acid strand, which is complementary to the existing ribonucleic acid strand. The thus produced strand is named “first strand of cDNA.” This cDNA can be used in a PCR reaction, whereby it results in the use of either random primers or else specific primers to generate an amplificat. Shi et al. teaches especially the miRNA detection via an oligo-dT adapter-primer, whereby an adapter of the specific primer is used in the PCR (Shi, R., and Chiang, V. L. (Shi, R. et al., Facile Means for Quantifying microRNA Expression by Real-Time PCR, Biotechniques, 2005, 39, 519-25).

This only recently published process has decisive drawbacks relative to the above-mentioned special ribonucleic acid molecules.

Thus, the two-stage process in general may involve an introduction of contaminants. The purification step leads to losses of rare RNAs. The two-stage process requires an inactivation of the first enzyme as well as an incubation time for the first enzyme and the second enzyme, which together results in a very great time expenditure. In addition, the two-stage process has the drawback that a danger of confusion of samples can then occur when two or more samples are treated at the same time. As is known from the prior art, ribonucleic acids are relatively sensitive as far as the attack of nucleases is concerned. The two-stage process, in particular the step of purification after the first process, involves the danger that nucleases are introduced. Ultimately, two or more steps always lead to the fact that the danger of pipetting errors increases.

SUBJECT OF THE INVENTION

It is thus the object of this invention to prepare a process that makes possible the cDNA synthesis, prevents contaminants as much as possible, is less time-consuming, minimizes the danger of confusion of the samples, minimizes the danger of the introduction of nucleases, and finally excludes the danger of pipetting errors as much as possible.

This object is achieved by a process for synthesis of a cDNA in a sample, in an enzymatic reaction, whereby the process comprises the following steps:

(a) Simultaneous preparation of a first enzyme with polyadenylation activity, a second enzyme with reverse transcriptase activity, a buffer, at least one ribonucleotide, at least one deoxyribonucleotide, an anchor oligonucleotide, (b) addition of a sample that comprises a ribonucleic acid, and (c) incubation of the agents of steps (a) and (b) in one or more temperature steps, which are selected such that the first enzyme and the second enzyme show activity.

Up until today, there have been concerns about a combination of the enzymatic polyadenylation and the reverse transcriptase being technically possible. This is shown in that even more recently, i.e., after discovery of microRNAs and snoRNAs, which represent a special molecular-biological challenge as regards analysis and isolation, the enzymatic reactions were always performed in succession (Want, J. F., et al., Identification of 20 microRNAs from Oryza sativa, Nucleic Acid Res., 2004, 32, 1688-95; Shi, R. and Chiang, V. L., Facile Means for Quantifying microRNA Expression by Real-Time PCR, Biotechniques, 2005, 39, 519-25; Fu, H., et al., Identification of Human Fetal Liver miRNAs by a Novel Method; FEBS Lett, 2005, 579, 3849-54; Chen, C. L. et al., The High Diversity of snoRNAs in Plants: Identification and Comparative Study of 120 snoRNA Genes from Oryza Sativa, Nucleic Acids Res, 2003, 31, 2601-13; Botero, L. M. et al., Poly(A) Polymerase Modification and Reverse Transcriptase PCR Amplification of Environmental RNA, Appl. Environ Microbial, 2005, 71, 1267-75). Surprisingly enough, both processes, i.e., the polyadenylation and reverse transcription, have already been known to one skilled in the art for a long time (Sano, H., and Feix, G., Terminal Riboadenylate Transferase from Escherichia coli. Characterization and Application, Eur. J. Biochem., 1976, 71, 577-83). In general, according to the poly-A-tailing step, one skilled in the art has purified the reaction product (Shi, R., et al., Facile Means for Quantifying microRNA Expression by Real-Time PCR, Biotechniques, 2005, 39, 519-25). The reason for this lies both in the clearly different compositions of the reaction buffers and the substrates that are required for the reaction.

Another subject of this invention is to prepare a simple process that makes the cDNA synthesis possible and couples this reaction optionally with a third enzymatic reaction, which allows the specific detection of the generated cDNA in the same reaction vessel. By a very simple handling, this “3-in-1” process shows special advantages when a large number of samples are to be analyzed in one or a few analytes. The reason is that, e.g., coupled to a real-time PCR, a very quick and simple process shows a large number of samples to be analyzed. Additional handling steps and contaminations are to be prevented as much as possible, by which it is less time-consuming, the danger of confusion of the samples is minimized, the danger of the introduction of nucleases is minimized, and ultimately, the danger of pipetting errors is excluded as much as possible.

The object of the “3-in-1” reaction is achieved by a process for the synthesis of a cDNA in a sample, in an enzymatic reaction, followed by another enzymatic reaction, optionally an amplification, optionally coupled to the detection, either in real-time during the amplification or downstream, whereby the process comprises the following steps: (a) simultaneous preparation of a first enzyme with polyadenylation activity, a second enzyme with reverse transcriptase activity, a buffer, at least one ribonucleotide, at least one deoxyribonucleotide, an anchor oligonucleotide, at least a third enzyme with nucleic acid-synthesis activity, at least one primer, and optionally a probe, (b) addition of a sample that comprises a ribonucleic acid, and (c) incubation of the agents of steps (a) and (b) in one or more temperature steps, which are selected such that the first and second enzyme show activity, and optionally the third enzyme is active or inactive. Optionally one or more temperature steps follow, in which the first and second enzymes are less active or inactive, and the third enzyme is active.

The substrate of the poly-(A)-polymerase that is used in vivo is adenosine triphosphate (ATP). For some poly-(A)-polymerases, it was shown that even attaching a short tail to other NTPs as a substrate can be possible (Martin, G., and Keller, W., Tailing and 3′-End Labeling of RNA with Yeast Poly(A) Polymerase and Various Nucleotides, RNA, 1998, 4, 226-30).

Surprisingly enough, the inventors of this invention had discovered that it is possible, under certain requirements, to be able to execute the two still very different enzymatic reactions simultaneously in one reaction vessel. In a preferred embodiment of the invention, the sample is a ribonucleic acid, which is selected from the group that comprises prokaryotic ribonucleic acids, eukaryotic ribonucleic acids, viral ribonucleic acids, ribonucleic acids whose origin is an archae-organism, microribonucleic acids (miRNA), small nucleolar ribonucleic acids (snoRNA), messenger ribonucleic acid (mRNA), transfer-ribonucleic acids (tRNA), non-polyadenylated ribonucleic acids in general, as well as ribosomal ribonucleic acids (rRNA). Moreover, a mixture of two or more of the above-mentioned ribonucleic acids. In the sample, of course, poly-A RNA can also already be contained.

In an especially preferred embodiment of this invention, the sample is a ribonucleic acid, which is selected from the group that comprises prokaryotic ribonucleic acids, miRNA, snoRNA and rRNA. In the most preferred embodiment of this invention, the sample comprises a ribonucleic acid, which is selected from the group that comprises miRNA and snoRNA. Other mixed samples that consist of different amounts of ribonucleic acids of different types associated with other substances are preferred.

In addition, the inventors of this invention have discovered that it is possible, under certain conditions, to be able to execute the two still very different enzymatic reactions simultaneously in one reaction vessel as well as to couple the latter in addition to a third enzymatic reaction for specific detection of the generated cDNA, which is preferably a nucleic acid-synthesis activity. In a preferred embodiment of the invention, the sample is a ribonucleic acid, which is selected from the group that comprises prokaryotic ribonucleic acids, eukaryotic ribonucleic acids, viral ribonucleic acids, ribonucleic acids whose origin is an archae-organism, microribonucleic acids (miRNA), small nucleolar ribonucleic acids (snoRNA), messenger ribonucleic acid (mRNA), transfer-ribonucleic acids (tRNA), and non-polyadenylated ribonucleic acids in general, as well as ribosomal ribonucleic acids (rRNA). Moreover, a mixture of two or more of the above-mentioned ribonucleic acids. In the sample, of course, poly-A RNA can also already be contained.

In an especially preferred embodiment of this invention, the sample is a ribonucleic acid that is selected from the group that comprises prokaryotic ribonucleic acids, miRNA, snoRNA and rRNA. In the most preferred embodiment of this invention, the sample comprises a ribonucleic acid, which is selected from the group that comprises miRNA and snoRNA. Other mixed samples that consist of different amounts of ribonucleic acids of different types associated with other substances are preferred. Based on these advantages of the process according to the invention, the inventors could show that it is possible to prepare and to characterize miRNAs efficiently and without contamination.

In one embodiment of the invention, the anchor oligonucleotide is a homopolymer oligonucleotide, which is selected from the group that comprises a poly-(A)-oligonucleotide, poly-(C)-oligonucleotide, poly-(T)-oligonucleotide, poly-(G)-oligonucleotide, poly-(U)-oligonucleotide, poly-(A)-oligonucleotide additionally comprising a 5′-tail, poly-(C)-oligonucleotide additionally comprising a 5′-tail, poly-(T)-oligonucleotide additionally comprising a 5′-tail, poly-(G)-oligonucleotide additionally comprising a 5′-tail and poly-(U)-oligonucleotide additionally comprising a 5′-tail. A poly-(T)-oligonucleotide, which optionally, as already explained above, additionally can have a 5′-tail, is preferred.

The anchor oligonucleotide according to the invention is generally between 6 and 75 nucleotides long. However, it can be up to about 150 nucleotides long. If the anchor oligonucleotide is synthetic, the maximum length follows from the technical limitations of the DNA synthesis. The anchor oligonucleotide optionally comprises a 5′-tail and/or an anchor sequence. A 5′-tail is an additional nucleotide sequence on the 5′-end of the oligonucleotide, which is used, for example, to introduce a cloning sequence, primer and/or probe-binding sites or any other sequence. The identification of suitable sequences for the 5′-tail is possible for one skilled in the art based on the requirements of the respective application.

On the 3′-end of the anchor oligonucleotide, an additional anchor sequence, typically with a length of one to five additional nucleotides, can be contained. The anchor sequence can have a length of at least one base, whereby the first position in a preferred embodiment is a degenerated base, which contains all bases except for the base that is used in the homopolymer portion of the anchor oligonucleotide. After that, other bases can follow. The latter can also be degenerated. In one preferred embodiment here, the use of N wobbles is useful, whereby N=A, C, G, T or corresponding analogs.

Normally, the anchor oligonucleotide is a deoxyribonucleic acid (DNA). The anchor oligonucleotide, however, can also be a peptide nucleic acid (PNA). Locked nucleic acids (LNA), phosphorus thioate-deoxyribonucleic acids, cyclohexene-nucleic acids (CeNA), N3′-P5′-phosphoramedites (NP), and tricyclo-deoxyribonucleic acids (tcDNA) are also possible. An anchor oligonucleotide, which is a deoxyribonucleic acid (DNA), is preferred, however. Mixtures of RNA and DNA or one or more of the modified nucleic acids or analogs, as well as other modifications, such as corresponding base analogs, which are able to hybridize with RNA or DNA under the selected conditions, are possible. In one especially preferred embodiment, the anchor oligonucleotide is a poly-(T)-oligonucleotide, which additionally comprises a 5′-tail, is a deoxyribonucleic acid, is 15-150 nucleotides long, and is present as a mixture. On the 3′-end of the anchor oligonucleotide, an additional anchor sequence typically with a length of one to five additional nucleotides can be contained. The anchor sequence can have a length of at least one base, whereby the first position in a preferred embodiment is a degenerated base, which contains all bases except for the base that is used in the homopolymer portion of the anchor oligonucleotide. After that, other bases can follow. The latter can also be degenerated. Here, in a preferred embodiment, the use of N wobbles is useful, whereby N=A, C, G, T or corresponding analogs.

By way of example, the following anchor oligonucleotides according to the invention can be mentioned:

Example 1 (SEQ ID NO: 10): 5′ TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CC (T)xVVN 3′ Example 2 (SEQ ID NO: 11): 5′ AACGAGACGACGACAGAC(T)x VN 3′ Example 3 (SEQ ID NO: 12): 5′ AACGAGACGACGACAGAC(T)x V 3′ Example 4 (SEQ ID NO: 13): 5′ AACGAGACGACGACAGAC(T)x N 3′ Example 5 (SEQ ID NO: 14): 5′ AACGAGACGACGACAGAC(T)x NN 3′ Example 6 (SEQ ID NO: 15): 5′ AACGAGACGACGACAGAC(T)x VNN 3′ Example 7 (SEQ ID NO: 16): 5′ AACGAGACGACGACAGAC(T)x VNNN 3′ Example 8 (SEQ ID NO: 17): 5′ AACGAGACGACGACAGAC(T)x NNN 3′ Example 9 (SEQ ID NO: 18): 5′ TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CC(T)x VN 3″ Example 10 (SEQ ID NO: 19): 5′ TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CC(T)x VNN 3′

-   -   X is preferably 10 to 30 bases.     -   V and N are from the single letter code for degenerated bases,         V=A, C, G; N=A, C, G, T.

The identification of other suitable 5′-tail sequences is possible to one skilled in the art.

The optional 5′-tail comprises additional 1-100 nucleotides, which can be used for the following analyses. Thus, in a preferred embodiment, the 5′-tail can contain the binding sequence for an oligonucleotide, such as, e.g., one or more DNA probes and/or one or more PCR primers. The sequences that are used for the 5′-tail are preferably selected such that the latter are compatible with the process according to the invention. This comprises, e.g., the selection of those sequences that do not cause any undesirable secondary reactions, both in the process according to the invention and in the subsequent analysis process.

According to the invention, anchor oligonucleotides are shown in FIG. 12.

In principle, the enzymatic reaction according to the invention can take place on a vehicle or in a container, i.e., the reaction can take place in a reaction vessel. Such a reaction vessel can be a reaction tube or, for example, a microtiter plate. The reaction can take place on a chip. If it takes place on a chip, one or more components can be immobilized. The reaction can take place on a test strip or in a microfluidic system. The most varied embodiments relative to the vehicle or container are known to one skilled in the art.

In a preferred embodiment, the ribonucleotide is an adenosine-5′-triphosphate, a thymidine-5′-triphosphate, a cytosine-5′-triphosphate, a guanine-5′-triphosphate and/or a uracil-5′-triphosphate. The ribonucleotide can also be a base analog. The ribonucleotide can be modified or labeled. In principle, it is essential that the ribonucleotide can be reacted by the enzyme in the polyadenylation activity as substrate.

The deoxyribonucleotide according to the invention can be selected from the group that comprises a deoxyadenosine-5′-triphosphate (dATP), a deoxythymine-5′-triphosphate (dTTP), a deoxycytosine-5′-triphosphate (dCTP), a deoxyguanosine-5′-triphosphate (dGTP), a deoxayuracil-5′-triphosphate (dUTP) as well as modified deoxyribonucleotides and labeled deoxyribonucleotides. Applications are also conceivable in which in addition to or in exchange, one or more deoxyribonucleotides, which contain a universal base or a base analog, are used. It is essential for the implementation of the invention that the deoxyribonucleotides that are used allow a cDNA synthesis.

According to the invention, it is preferred if dATP, dCTP, dTTP, and dGTP are present together as a mixture.

According to the invention, deoxyuracil-5′-triphosphate can also be used in the mixture. This can be combined with an enzymatic reaction that takes place after the actual reaction and that uses the uracil-DNA-glycosilase and cannot degrade further used enzymatically produced reaction product.

If a deoxyribonucleotide is labeled, the labeling can be selected from the group that comprises ³²P, ³³P, ³⁵S, ³H; a fluorescent dye, such as, for example, fluorescein isothiocyanate (FITC), 6-carboxyfluorescein (FAM), xanthene, rhodamine, 6-carboxy-2′,4′,7′,4,7-hexachlorofluorescein (HEX), 6-carboxy-4′,5′-dichloro-2′,7′-dimethoxy fluorescein (JOE), N,N,N′,N′-tetramethyl-6-carboxyrhodamine (TAMRA), 6-carboxy-X-rhodamine (ROX), 5-carboxyrhodamine-6G (R6G5), 6-carboxyrhodamine-6G (RG6), rhodamine 110; coumarins, such as umbelliferones; benzimides, such as Hoechst 33258; phenanthridines, such as Texas Red, ethidium bromides, acridine dyes, carbazole dyes, phenoxazine dyes, porphyrine dyes, polymethine dyes; cyanine dyes, such as Cy3, Cy5, Cy7, BODIPY dyes, quinoline dyes and alexa dyes. Other labels such as the inclusion of biotin or one or more haptens, such as, e.g., digoxigenin, which allow a direct or indirect detection of the nucleic acid. Indirect detection, such as, e.g., via antibodies, which in turn, e.g., enzymatic detection via an enzyme coupled to an antibody. Also, via the introduction of nanoparticles, which are coupled to, e.g., antibodies or an affinity ligand, an indirect detection is possible.

A modification of the deoxyribonucleotide can also be carried out via the 5′-phosphate, which allows a simpler cloning. By including reactive groups, such as, e.g., an amino linker (also biotin), the deoxyribonucleotide can be, e.g., immobilized, or a direct or indirect detection can be made available.

Especially preferred modifications are selected from the group that comprises fluorescence dyes, haptens, 5′-phosphate, 5′-biotin, and 5′-amino linkers.

According to the invention, the concentration of a deoxyribonucleotide in the reaction is at least 0.01 mmol and at most 10 mmol. This concentration information is the concentration of the individual deoxyribonucleotide. In one of the preferred embodiments, the deoxyribonucleotides, in each case dATP, dCTP, dGTP and dTTP, are present at a concentration of 0.2 mmol to 2 mmol. This concentration information is the concentration of the individual deoxyribonucleotide in the mixture. In an especially preferred embodiment of the invention, the individual deoxyribonucleotide, dATP, dCTP, dGTP and dTTP, is present at a concentration of 0.5 mmol in each case.

Surprisingly enough, the inventors have determined that the one-step enzyme reaction, as it is the subject of this invention, can take place in a narrow buffer-pH range of 6 to 10 with the presence of magnesium ions (Mg²+). Thus, a pH of 6 to 10 is present in a preferred embodiment.

In an especially preferred embodiment, the buffer according to the invention has a pH of 6.8 to 9.

In another embodiment of the invention according to the invention, the buffer according to the invention comprises additional ions, which can be selected from the group that comprises Mn²+, K+, NH⁴+, and Na+.

Buffers according to the invention contain, for example, MgCl₂, MgSO₄, magnesium acetate, MnCl₂, KCl, (NH₄)zS0₄, NH₄Cl, and NaCl. As buffer substances, tris, tricine, bicine, HEPES, as well as other buffer substances that are in the pH range according to the invention or mixtures of two or more appropriate buffer substances are suitable.

A number of enzymes with polyadenylation activity are known to one skilled in the art. According to the invention, the latter are selected from the group that comprises enzymes of prokaryotic origin, eukaryotic origin, viral origin and archae origin as well as also enzymes of plant origin.

A polyadenylation activity in terms of this invention is an enzymatic activity that uses the 3′-end of a ribonucleic acid as a substrate and is able to add enzymatic ribonucleotides, specifically preferably at least 10 to 20 ribonucleotides, to this 3′-end in a suitable buffer. In a preferred embodiment, the enzyme is an enzyme that is able to use adenosine-5′-triphosphate as a substrate. According to the invention, the latter comprises enzymes and reaction conditions that have a polyadenylation activity in terms of the invention when using single-strand and double-strand RNA, e.g., hairpin RNA, such as, e.g., pre-miRNA. Based on the RNA to be analyzed, one skilled in the art can select enzymes and reaction conditions such that either single-strand RNAs (e.g., mature miRNAs), or double-strand RNAs (e.g., pre-miRNAs) or both are made available for analysis.

In general, a polyadenylation activity in terms of the invention is a transcriptase activity.

In a preferred embodiment, the enzyme with polyadenylation activity is an enzyme that is selected from the group that comprises poly-(A)-polymerase from Escherichia coli, poly-(A)-polymerase from yeast, poly-(A)-polymerase from cattle, poly-(A)-polymerase from frogs, human poly-(A)-polymerase, and plant poly-(A)-polymerase. Others are known to one skilled in the art or can be newly identified by the analysis of homology in known poly-(A)-polymerases. In an especially preferred embodiment, the enzyme with polyadenylation activity is a poly-(A)-polymerase from Escherichia coli.

The enzyme with reverse transcriptase activity according to the invention is selected according to the invention from the group that comprises enzymes from viruses, bacteria, archae-bacteria and eukaryotes, in particular from thermostable organisms. These also include, e.g., enzymes from Intrans, retrotransposons or retroviruses. An enzyme with reverse transcriptase activity is an enzyme, according to the invention, which is able to incorporate deoxyribonucleotides in a complementary way in a ribonucleic acid on the 3′-end of a deoxyoligonucleotide or ribooligonucleotide that is hybridized on the ribonucleic acid under suitable buffer conditions. This comprises, on the one hand, enzymes that of course have this function but also enzymes that obtain such a function only by changing their gene sequence, such as, e.g., mutagenesis, or by corresponding buffer conditions.

Preferred is the enzyme with reverse transcriptase activity, an enzyme that is selected from the group that comprises HIV Reverse Transcriptase, M-MLV Reverse Transcriptase, EAIV Reverse Transcriptase, AMY Reverse Transcriptase, Thermus thermophilus DNA polymerase I, M-MLV RNAse H, Superscript, Superscript II, Superscript Ill, MonsterScript (Epicenter), Omniscript, Sensiscript Reverse Transcriptase (Qiagen), ThermoScript and Thermo-X (both Invitrogen). According to the invention, enzymes can also be used that as enzymes have reverse transcriptase only after a modification of the gene sequence. A reverse transcriptase activity that has elevated accuracy can also be used. By way of example, e.g., AccuScript Reverse Transcriptase (Stratagene) can be mentioned here. It is evident to one skilled in the art that even the use of mixtures of two or more enzymes with reverse transcriptase activity is possible.

It is known to one skilled in the art that most enzymes with reverse transcriptase activity require a divalent ion. Thus, in a preferred embodiment as already described above, a divalent ion is present in those enzymes that require a divalent ion. Mg²+ and Mn² are preferred.

Preferred combinations of enzymes are HIV Reverse Transcriptase or M-MLV Reverse Transcriptase or EAIV Reverse Transcriptase or AMY Reverse Transcriptase or Thermus thermophilus DNA polymerase I or M-MLV RNAse H, Superscript, Superscript II, Superscript III or MonsterScript (Epicenter) or Omniscript Reverse Transcriptase (Qiagen) or Sensiscript Reverse Transcriptase (Qiagen), ThermoScript, Thermo-X (both Invitrogen) or a mixture of two or more enzymes with reverse transcriptase activity and poly-(A)-polymerase from Escherichia coli. In addition, HIV Reverse Transcriptase or M-MLV Reverse Transcriptase or EAIV Reverse Transcriptase or AMY Reverse Transcriptase or Thermus thermophilus DNA Polymerase I or M-MLV RNAse H, Superscript, Superscript II, Superscript III or MonsterScript (Epicenter) or Omniscript Reverse Transcriptase (Qiagen) or Sensiscript Reverse Transcriptase (Qiagen), ThermoScript, Thermo-X (both Invitrogen) or a mixture of two or more enzymes with reverse transcriptase activity and poly-(A)-polymerase from yeast.

It is known to one skilled in the art that high temperatures in reverse transcription have the effect that problems with secondary structures do not play a decisive role. Moreover, high temperatures in certain enzymes have the effect that the specificity of reverse transcription increases such that false pairs and false priming are suppressed. Thus, a reverse transcriptase, which is thermophilic, is used in an embodiment of this invention. An enzyme that has an optimum nucleic acid synthesis activity at between 45° C. and 85° C. is preferred, more preferred between 55° C. and 80° C., and most preferred between 60° C. and 75° C. Thermus thermophilus (Tth) DNA polymerase I is preferred.

If the enzyme with polyadenylation activity is a non-thermophilic enzyme and the enzyme with reverse transcriptase activity is a thermophilic enzyme, the process can be carried out in several temperature steps according to the invention, whereby the first temperature step allows a temperature to be used that is the optimum temperature for the enzyme with polyadenylation activity, and the second temperature step allows a temperature to be used that is the optimum temperature for the enzyme with reverse transcriptase activity.

If, for example, the AMY reverse transcriptase is used, the second temperature step takes place at 42° C., while the first temperature step, which has primarily the activity of the enzyme with polyadenylation activity, takes place at a temperature of 37° C. Implementation at a constant temperature is also possible, however.

One skilled in the art is able to select the temperatures so that the respective enzyme activities have an impact. If, for example, a combination of poly-(A)-polymerase from Escherichia coli accompanied by DNA polymerase from Thermus thermophilus is used, the course of the temperatures appears as follows: first, it is incubated at 37° C. and then at 55 to 70° C. According to the invention, a non-thermostable enzyme can thus be combined with a thermostable enzyme. In this case, the temperature steps then depend on which of the two enzymes has polyadenylation activity. According to the invention, it is preferred that the enzyme with reverse transcriptase reactivity be thermostable. In the opposite case, and this is plausible to one skilled in the art, it may be that by the incubation at a higher temperature in the polyadenylation step, the enzyme with reverse transcriptase activity is partially or completely inactivated. Thus, it is also preferred if the two enzymes are thermostable.

In addition, it is known to one skilled in the art that the enzymes are processive to very different degrees, so that one skilled in the art can combine enzymes with different processivity in such a way that templates of varying lengths are readily converted into cDNA in different ways. By using corresponding amounts of the respective enzymes, of one or more suitable incubation temperatures and incubation times, it is possible for one skilled in the art to achieve satisfactory results.

The process according to the invention preferably comprises additional poly-(C)-polynucleotides. The process according to the invention especially preferably comprises additional poly-(C)-polyribonucleotides. Preferably, 1 ng to 300 ng of poly-(C)-polyribonucleotides for each 20 μl is incorporated, preferably 10 ng to 150 ng of poly-(C)-polyribonucleotides for each 20 μl of reaction is incorporated, especially preferably 25 ng to 100 ng of poly-(C)-polyribonucleotides for each reaction is incorporated, and most preferably 50 ng to 75 ng of poly-(C)-polyribonucleotides for each 20 μl of reaction is incorporated.

The reaction according to the invention can comprise additional reagents, such as, for example, volume excluder, a single-strand binding protein, DTT and/or competitor nucleic acids.

If a volume excluder is used, the latter is selected from the group that comprises dextran, and polyethylene glycol, and in EP 1411133A1, volume excluders according to the invention are mentioned.

In a preferred embodiment, the competitor-nucleic acid is a homopolymer ribonucleic acid, most preferably polyadenoribonucleic acid. Examples are disclosed in U.S. Pat. No. 6,300,069.

The process according to the invention preferably comprises additional poly-(C)-polynucleotides. The process according to the invention especially preferably comprises additional poly-(C)-polyribonucleotides. Preferably, 1 ng to 300 ng of poly-(C)-polyribonucleotides is incorporated for each 20 μl; preferably 10 ng to 150 ng of poly-(C)-polyribonucleotides is incorporated for each 20 μl of reaction; especially preferably, 25 ng to 100 ng of poly-(C)-polyribonucleotides is incorporated for each reaction; and most preferably 50 ng to 75 ng of poly-(C)-polyribonucleotides is incorporated for each 20 μl of reaction.

It is obvious to one skilled in the art that it may be advantageous to prevent the competitor-nucleic acid itself from being used as a substrate for the poly-(A)-polymerase activity. A possible solution is the blocking of the 3′ OH group of the competitor-nucleic acid. Corresponding solutions, such as, e.g., use of a 3′ phosphate, incorporation of a dideoxynucleotide or reverse bases, are known to one skilled in the art.

It is also obvious to one skilled in the art that it is advantageous to be able to prevent the competitor-nucleic acid itself from being used as a substrate for the reverse transcriptase activity. This can be ensured by selecting a competitor-nucleic acid that cannot be converted into cDNA under the given reaction conditions, e.g., since the primers that are used cannot hybridize onto the latter. Another possible solution is the blocking of the 3′ OH group of the competitor-nucleic acid. Corresponding solutions, such as, e.g., use of a 3′ phosphate, incorporation of a dideoxynucleotide or reverse bases, are known to one skilled in the art.

In addition, the invention relates to a reaction mixture that comprises a first enzyme with polyadenylation activity, a second enzyme with reverse transcriptase activity, optionally a buffer, optionally at least one ribonucleotide, optionally at least one deoxyribonucleotide and optionally one anchor oligonucleotide. The anchor oligonucleotide preferably comprises a homopolymer portion, an anchor sequence and/or a tail. The reaction mixture additionally preferably comprises random primers. The additional use of random primers has the advantage that even 5′-ends of long transcripts are efficiently converted, which is important in quantitative analyses. The reaction mixture can contain the same agents as are used for the process according to the invention.

In an embodiment of the invention, the anchor oligonucleotide is a homopolymer oligonucleotide, which is selected from the group that comprises a poly-(A)-oligonucleotide, poly-(C)-oligonucleotide, poly-(T)-oligonucleotide, poly-(G)-oligonucleotide, poly-(U)-oligonucleotide, poly-(A)-oligonucleotide additionally comprising a 5′-tail, poly-(C)-oligonucleotide additionally comprising a 5′-tail, poly-(T)-oligonucleotide additionally comprising a 5′-tail, poly-(G)-oligonucleotide additionally comprising a 5′-tail and poly-(U)-oligonucleotide additionally comprising a 5′-tail. Preferred is a poly-(T)-oligonucleotide, which optionally in addition can have a 5′-tail as already explained above.

The anchor oligonucleotide according to the invention is generally between 6 and 75 nucleotides long. It can be up to about 150 nucleotides long, however. If the anchor oligonucleotide is synthetic, the maximum length is produced from the technical limitations of the DNA synthesis. The anchor oligonucleotide optionally comprises a 5′-tail and/or an anchor sequence. A 5′-tail is an additional nucleotide sequence on the 5′-end of the oligonucleotide, which, for example, in this case is used to insert a cloning sequence, primer and/or probe-binding sites, or any other sequence. The identification of suitable sequences for the 5′-tail is possible for one skilled in the art based on the requirements of the respective application.

At the 3′-end of the anchor oligonucleotide, an additional anchor sequence typically can be contained with a length of one to five additional nucleotides. The anchor sequence can have a length of at least one base, whereby the first position in a preferred embodiment is a degenerated base, which contains all bases except for the base that is used in the homopolymer portion of the anchor oligonucleotide. Then, additional bases can follow. The latter can also be degenerated. In a preferred embodiment, the use of N wobbles is useful here, whereby N=A, C, G, T or corresponding analogs.

The optional 5′-tail additionally comprises 1-100 nucleotides, which can be used for subsequent analyses. Thus, in a preferred embodiment, the 5′-tail can contain the binding sequence for an oligonucleotide, such as, e.g., one or more DNA probes and/or one or more PCR primers. The sequences that are used for the 5′-tail are preferably selected such that the latter are compatible with the process according to the invention. This comprises, e.g., the selection of those sequences that do not cause any undesirable secondary reactions, both in the process according to the invention and in subsequent analytical processes.

The reaction mixture according to the invention comprises the anchor oligonucleotide according to the invention, which has a length of between 10 and 150 nucleotides, and optionally at the 3′-end, carries an anchor sequence according to the invention that is one to five nucleotides long. The reaction mixture according to the invention comprises the anchor oligonucleotide, which, as described above, for example, is a deoxyribonucleic acid (DNA), a peptide nucleic acid (PNA) or a locked nucleic acid (LNA). In a preferred embodiment, the reaction mixture according to the invention comprises an anchor oligonucleotide according to the invention, which is a poly-(T)-oligonucleotide and in addition carries a 5′-tail, whereby the oligonucleotide is a deoxyribonucleic acid, which is 10 to 75 nucleotides long and is present as a mixture, whereby on the 3′-end, an anchor sequence is present, consisting of one nucleotide in each case, which is selected from the group that comprises A, G and C, optionally followed by one to five additional nucleotides that comprise all four bases A, C, G and T or corresponding analogs.

Anchor oligonucleotides of the reaction mixture according to the invention are shown in FIG. 12.

The reaction mixture according to the invention also comprises at least one ribonucleotide as they were described above for the process according to the invention. In particular, the reaction mixture according to the invention comprises at least one ribonucleotide that is selected from ATP, TTP, CTP, GTP, UTP or corresponding base analogs. The ribonucleotides can optionally be modified or labeled as described above. The reaction mixture according to the invention comprises deoxyribonucleotides, as it was described for the process according to the invention. In particular, the reaction mixture according to the invention comprises one or more deoxyribonucleotides, such as, for example, dATP, dCTP, dGTP, dUTP, and/or dTTP. In a preferred embodiment, a mixture of deoxyribonucleotides, which allow a cDNA synthesis, is used. These deoxyribonucleotides can optionally be modified or labeled.

If a deoxyribonucleotide of the reaction mixture according to the invention is labeled, the labeling can be selected from the group that comprises ³²P, ³³P, ³⁵S, ³H, a fluorescent dye such as, for example, fluorescein isothiocyanate (FITC), 6-carboxyfluorescein (FAM), xanthene, rhodamine, 6-carboxy-2′,4′,7′,4,7-hexachlorofluorescein (HEX), 6-carboxy-4′,5′-dichloro-2′,7′-dimethoxy fluorescein (JOE), N,N,N′,N′-tetramethyl-6-carboxyrhodamine (TAMRA), 6-carboxy-X-rhodamine (ROX), 5-carboxyrhodamine-6G (R6G5), 6-carboxyrhodamine-6G (RG6), rhodamine 110; Cy3, Cy5, Cy7, coumarins, such as umbelliferone, benzimides, such as Hoechst 33258; phenanthridines, such as Texas Red, ethidium bromides, acridine dyes, carbazole dyes, phenoxazine dyes, porphyrin dyes, polymethine dyes, cyanine dyes, such as Cy3, Cy5, BODIPY dyes, quinoline dyes and Alexa dyes. Other labels, such as the insertion of biotin or one or more haptens, such as, e.g., digoxigenin, which allow a direct or indirect detection of the nucleic acid. Indirect detection, such as, e.g., via antibodies, which in turn, e.g., enzymatic detection via an enzyme coupled to an antibody. Also, via the introduction of nanoparticles, which are coupled to, e.g., antibodies or an affinity ligand, an indirect detection is possible.

The reaction mixture according to the invention in each case comprises a deoxyribonucleotide at a concentration of 0.01 mmol to 10 mmol. The individual deoxyribonucleotide A, C, G and T is preferably present at a concentration of 0.2 mmol to 2 mmol in each case. It is especially preferred if the deoxyribonucleotides A, C, G and T are present together. Each individual one is present in this preferred embodiment at a concentration of 0.5 mmol.

In addition, the reaction mixture according to the invention comprises a buffer. This buffer has a pH of 6 to 10. In addition, in the reaction mixture according to the invention, Mg²+ ions are found. In an especially preferred embodiment, the reaction mixture according to the invention has a buffer with a pH of 6.8 to 9. The reaction mixture can further comprise additional ions, which can be selected from the group that comprises Mn²+, K+, NH⁴+, and Na+. The presence of two different enzyme activities is essential for the reaction mixture according to the invention. The reaction mixture according to the invention comprises at least a first enzyme activity with polyadenylation activity and secondly, a second enzyme activity with reverse transcriptase activity. The preferred embodiments of these activities were already described above for the process. In addition, like the process above, the reaction mixture can comprise additional substances, such as, for example, a volume excluder, a single-strand binding protein, DTT, or one or more competitor-nucleic acids.

If a volume excluder is used, it is preferred that the latter be selected from the group that comprises dextran and polyethylene glycol. Other volume excluders according to this invention are found in EP1411133A 1.

If the reaction mixture optionally comprises a competitor-nucleic acid, the latter is selected from the group that comprises homopolymer ribonucleic acids and polyadenoribonucleic acid. Other competitor-nucleic acids according to the invention are disclosed in U.S. Pat. No. 6,300,069.

The reaction mixture according to the invention preferably comprises additional poly-(C)-polynucleotides. The reaction mixture according to the invention especially preferably comprises additional poly-(C)-polyribonucleotides. 1 ng to 300 ng of poly-(C)-polyribonucleotides is preferably incorporated for each 20 μl, 10 ng to 150 ng of poly-(C)-polyribonucleotides is preferably incorporated for each 20 μl of reaction, 25 ng to 100 ng of poly-(C)-polyribonucleotides is especially preferably incorporated for each reaction, and 50 ng to 75 ng of poly-(C) polyribonucleotides is most preferably incorporated for each 20 μl of reaction.

In addition, the invention relates to a kit, comprising a reaction mixture, as it was described above. The reaction mixture is present in a preferred embodiment in a single reaction vessel. In another embodiment, the kit comprises a reaction vessel, comprising the enzyme with polyadenylation activity, the enzyme with reverse transcriptase activity, optionally the deoxyribonucleotides, optionally at least one ribonucleotide, optionally a buffer containing Mg²+, and optionally one or more oligodeoxyribonucleotides in terms of the invention. Optionally, the reaction vessel in the kit according to the invention can contain additional components, as they were indicated for the reaction mixture according to the invention. In addition, the kit can comprise a probe for the 5′-tail of the anchor oligonucleotide according to the invention. In addition, the kit can contain one or more additional deoxyribonucleotides, thus, e.g., a generic primer for detecting the tail sequence that is introduced by reverse transcription. The reaction mixture can be present in “pellet form,” thus, e.g., freeze-dried. Additional preparation processes, which do not contain, e.g., liquid forms, are known to one skilled in the art.

In addition, the kit can optionally be combined with reagents as they are necessary for the PCR reaction or real-time PCR reaction. These reagents are preferred for at least one PCR reaction, which allows the detection of at least one of the cDNAs generated in the process according to the invention.

In addition, the kit can comprise optional random primers as well as optionally one or more primers or primer/probes to detect additional target genes in singleplex or multiplex PCR reactions and/or real-time singleplex or multiplex PCR reactions.

The reaction mixture, the process according to the invention or the kit can contain additional target-specific primers. The length of the target-specific primer should be selected such that a specific detection in a PCR reaction is possible; the sequence of the target primer should be specific, such that a binding to only one spot in the generated cDNA sequence is possible. Normally, such a primer has a length of 15 to 30 nucleotides, preferably 17 to 25 nucleotides.

In an especially preferred embodiment, the reaction mixture comprises the enzyme with polyadenylation activity and the enzyme with reverse transcriptase activity as a two-enzyme pre-mix. In this especially preferred embodiment, the kit comprises the two-enzyme-premix-reaction mixture in a reaction vessel and in a separate vessel, a buffer, Mg²+, rNTP(s), dNTP(s), optionally one anchor oligonucleotide according to the invention, and optionally random primers, as well as, in addition, optionally a volume excluding reagent and/or a competitor-nucleic acid.

The process according to the invention can, as already explained above, take place in one or more temperature steps. In a preferred embodiment, the process according to the invention takes place in a single temperature step for the incubation and another temperature step for the inactivation of the enzyme. Thus, in a preferred embodiment of the incubation step in which the enzyme activity develops, it is about 37° C. The incubation time is approximately 1 to 120 minutes, preferably 5 to 90 minutes, more preferably 10 to 75 minutes, still more preferably 15 to 60 minutes, still more preferably 20 to 60 minutes to most preferably 50 to 70 minutes. Normally, excessive incubation time is not harmful. In another step that uses the denaturation of the enzymes, a temperature of at least 65° C. but at most 100° C. is used. Preferably, a temperature of about 80-95° C. is used. The denaturation takes place for a period of at least 1 minute, but for at most 30 minutes. In a preferred embodiment, it is denatured for a period of 5 minutes.

The process according to the invention for generating cDNA can subsequently comprise a polymerase chain reaction. If this is the case, a primer that is specific to the tail that is introduced during cDNA synthesis and/or a specific primer is preferably added to the reaction mixture according to the invention. The reaction mixture then also contains a thermostable DNA-polymerase in addition.

The PCR reaction that subsequently takes place can also be a quantitative PCR reaction. It can take place in an array, take place in a microfluid system, take place in a capillary or else be a real-time PCR. Other variants of the PCR are known to one skilled in the art and are equally comprised by the process according to the invention.

The invention also relates to a process for reverse transcription of RNA in DNA, whereby the process comprises the following steps: preparation of a sample that comprises RNA, addition of a first enzyme with reverse transcriptase activity, a buffer, at least one deoxyribonucleotide, an oligonucleotide, incubation of the agents in one or more temperature steps, which are selected such that the enzyme shows activity, whereby the reaction comprises additional poly-(C)-polynucleotides.

Preferably, the enzyme with reverse transcriptase activity is HIV Reverse Transcriptase, M-MLV Reverse Transcriptase, EAIV Reverse Transcriptase, AMY Reverse Transcriptase, Thermus thermophilus DNA Polymerase I, M-MLV RNAse H-Superscript, Superscript II, Superscript Ill, Monsterscript (Epicenter), Omniscript Reverse Transcriptase (Qiagen), Sensiscript Reverse Transcriptase (Qiagen), ThermoScript, Thermo-X (both Invitrogen) or a mixture of two or more enzymes with reverse transcriptase activity and poly-(A)-polymerase from Escherichia coli. Especially preferred is HIV Reverse Transcriptase.

The reaction preferably comprises poly-(C)-polyribonucleotides. 1 ng to 300 ng of poly-(C)-polyribonucleotides is incorporated for each 20 μl, preferably 10 ng to 150 ng of poly-(C)-polyribonucleotides is incorporated for each 20 μl of reaction, especially preferably 25 ng to 100 ng of poly-(C)-polyribonucleotides is incorporated for each reaction, and most preferably, 50 ng to 75 ng of poly-(C)-polyribonucleotides is incorporated for each 20 μl of reaction.

In a preferred embodiment of the invention, the sample is a ribonucleic acid that is selected from the group that comprises prokaryotic ribonucleic acids, eukaryotic ribonucleic acids, viral ribonucleic acids, ribonucleic acids whose origin is an archae organism, microribonucleic acids (miRNA), small nucleolar ribonucleic acids (snoRNA), messenger ribonucleic acid (mRNA), transfer-ribonucleic acids (tRNA), non-polyadenylated ribonucleic acids in general, as well as ribosomal ribonucleic acids (rRNA), and moreover, a mixture of two or more of the above-mentioned ribonucleic acids. In the sample, of course, poly-A RNA can also already be contained.

As a template, an RNA can be used that is selected from the group that comprises eukaryotic ribonucleic acids, mRNA, prokaryotic ribonucleic acids, miRNA, snoRNA and rRNA. In the most preferred embodiment of this invention, the sample comprises a ribonucleic acid that is selected from the group that comprises miRNA and snoRNA. Additional mixed samples from varying amounts of ribonucleic acids of varying types accompanied by other substances are preferred.

Based on these advantages of the process according to the invention, the inventor could show that it is possible to prepare and to identify miRNAs efficiently and without contamination. Small amounts of RNA in general can be readily reverse transcribed with the process.

The invention also relates to a kit for reverse transcription that comprises an enzyme with reverse transcriptase activity and poly-(C)-polynucleotides, preferably poly-(C)-polyribonucleotides.

In one embodiment, the RNA is first polyadenylated before the sample is reverse transcribed.

EXAMPLES Example 1

Demonstration of the feasibility of a coupled, one-stage process of a poly-A-reaction and reverse transcription in the same reaction vessel; effect of various buffers on the efficiency of the detection of a 22-mer RNA oligonucleotide.

In this experiment, the feasibility of a coupled, one-stage process of a poly-(A)-polymerase reaction and reverse transcription in the same reaction vessel should be demonstrated. For this purpose, the coupled one-stage process was performed under various conditions. This was, on the one hand, the buffer supplied with the poly-(A)-polymerase, and, on the other hand, the buffer supplied with the reverse transcriptase. In addition, a mixture of poly-(A)-polymerase and reverse transcriptase buffers was tested. As a control, the reaction was performed in a two-stage process in a way similar to FIG. 1A.

The reactions were put together as indicated in Table 1.

TABLE 1 Poly-A-Reaction and Reverse Transcription Batch 1 Batch 2 Batch 3 Batch 4 a/b a/b a/b a/b Data from the Final Concentrations Two-Stage Process Reagents PAP Buffer RT Buffer Mixture of the 1.) PAP 2.) RT Two Buffers Reaction Reaction 5x PAP Buffer 1x 1x 1x 10x RT Buffer 1x 1x 1x MnCl₂, 25 mmol Solution 2.5 mmol 2.5 mmol 2.5 mmol rATP, 10 mmol 1 mmol 1 mmol 1 mmol 1 mmol Poly-(A)-polymerase, 4 U 2 U 4 U 2 U 2 U/μl (0.2 U/μl) (0.1 U/μl) (0.2 U/μl) (0.2 U/μl) dNTP Mix (dA, dT, 0.5 mmol 0.5 mmol 0.5 mmol 0.5 mmol dG, dC, 5 mmol each) UniGAPdT Primer, 1 μmol 1 μmol 1 μmol 1 μmol 10 μmol RNase Inhibitor, 10 U 10 U 10 U 10 U 10 U/μl Sensiscript Reverse 1 μl 1 μl 1 μl 1 μl Transcriptase RNase-Free Water Variable Variable Variable Variable Variable a) mleu7a 2 × 10E9 2 × 10E9 2 × 10E9 2 × 10E9 10 μl of PAP Copies Copies Copies Copies Reaction 1.) b) Neg Control (H₂O H₂O H₂O H₂O H₂O instead of mleu7a) a) Corn RNA 50 ng 50 ng 50 ng 50 ng b) Neg Control (H₂O H₂O H₂O H₂O H₂O instead of Corn RNA) Total Volume 20 μl 20 μl 20 μl 10 μl 20 μl Incubation 1 Hour, 37° C. 1 Hour 37° C., 1 Hour, 37° C. 5 Minutes, 93° C. Then Another Hour at 5 Minutes, 93° C. 2.) RT Reaction PAP: Poly A Polymerase RT: Reverse Transcription rATP: Adenosine 5′-Triphosphate

For this purpose, the reagents indicated in Table 2 were used.

TABLE 2 Materials for the Poly-A-Reaction and Reverse Transcription Poly-(A)-Polymerase Ambion; Material Number 80 U: 2030 Sensiscript RT Kit Qiagen; Material Number 50rxn: 205211 Adenosine 5′-Triphosphate (rATP) Amersham; Material Number 25 μmol: 27- 2056-01 RNase Inhibitor Promega; Material Number: N2511 Uni GAP dT Primer 5′-TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CCT TTT TTT TTT TTT TTT TTT TTY VN-3′ (SEQ ID NO: 2) Corn RNA From 1 g of Ground Corn Husks with Qiagen RNeasy Mini Kit (Cat. No. 74106); Plant Protocol with lOx Upscale (Maxi Shredder and Column) mleu7a RNA Oligonucleotide 5′-VGA GGU AGU AGG UGG UAU AGU U-3′ (SEQ ID NO: 1)

In each case, reactions were conducted with templates (1a, 2a, 3a, 4a, all with a synthetic RNA oligonucleotide in a background of corn RNA) or without templates (1b, 2b, 3b, 4b, all were added to H₂0 instead of templates). The reactions without templates were conducted as controls for the possible occurrence of nonspecific background. Corn RNA was selected as background RNA since the sequence of the 22-mer RNA oligonucleotide to be detected does not occur in corn.

After the inactivation of the enzymes (see Table: 5 minutes at 93° C.), 2 μl each of the batches 1 alb to 4 alb was used as templates in a real-time PCR. The preparation of the real-time PCR was carried out in three-fold batches as indicated in Table 3 with QuantiTect SYBR Green PCR Kit (Catalog No. 204143) and the primers indicated in Table 4.

TABLE 3 Components for SYBR Green Real-Time PCR Final Concentration 2x SYBR Green PCR Master Mix 1x Hum Uni Primer, 10 μmol 0.5 μmol miRNA Primer let7/short, 10 μmol 0.5 μmol RNase-Free Water Variable PAP-/RT-Reaction 2 μl Final Reaction Volume 20 μl

TABLE 4 Materials for the SYBR Green PCR (Table 4 discloses SEQ ID Nos: 4 and 3, respectively, in order of appearance. QuantiTect SYBR Qiagen; Material Number: 204143 Green PCR Kit (200) let 7short 5′-GAG GTA GTA GGT TGT ATA G-3′ (Specific miRNA (SEQ ID NO: 4) Primer) Hum Uni Primer 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO: 3)

The sequence 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO:3) that is contained in the universal tail-primer Hum Uni Primer was described in US2003/0186288A 1.

The PCR protocol consisted of an initial reactivation of the HotStarTaq polymerase that is contained in the QuantiTect SYBR Green PCR Master Mix for 15 minutes at 95° C., followed by 40 cycles for 15 seconds at 94° C., 30 seconds at 52° C., and 30 seconds at 72° C. (see Table 5).

TABLE 5 PCR Protocol for SYBR Green Real-Time PCR PCR Initial Reactivation 15 Minutes, 95° C. Denaturation 15 Seconds, 94° C. 40x Annealing 30 Seconds, 52° C. Extension (Data Acquisition) 30 Seconds, 72° C. Melt Curve

The acquisition of the fluorescence data was carried out during the 72° C. extension step. The PCR analyses were performed with an ABI PRISM 7700 (Applied Biosystems) in a reaction volume of 20 μl.

The PCR products were then subjected to a melt curve analysis. The latter was performed on an ABI PRISM 7000 real-time PCR instrument.

TABLE 6 Results of a Real-Time PCR Analysis of the Batches from Table 1 Ct CV Detector PAP/RT Template Ct Agent in % SYBR 1) PAP Buffer a) mleu7a 25.64 Green 2 × 10{circumflex over ( )}8 Copies + 25.22 25.50 0.95 Corn cDNA, 5 ng 25.64 b) H₂O in PAP - No Ct RT Reaction No Ct No Ct No Ct 2) RT Buffer a) mleu7a 17.43 2 × 10{circumflex over ( )}8 Copies + 17.31 17.32 0.58 Corn cDNA, 5 ng 17.23 b) H₂O in PAP- No Ct RT Reaction No Ct No Ct No Ct 3) Mixture of a) mleu7a 30.41 Both Buffers 2 × 10{circumflex over ( )}8 Copies + 30.23 30.28 0.36 Corn cDNA, 5 ng 30.21 b) H₂O in PAP- No Ct RT Reaction No Ct No Ct No Ct 4) Two-Stage a) mleu7a 25.54 Process 2 × 10{circumflex over ( )}8 Copies + 25.74 25.64 0.39 Corn DNA, 5 ng 25.65 b) H₂O in PAP- No Ct RT Reaction No Ct No Ct No Ct

The identity of the PCR products was then examined with the aid of agarose-gel electrophoresis. For this purpose, 10 μl of each PCR reaction was loaded onto a 2% agarose gel colored with ethidium bromide and separated. 100 bp Lader (Invitrogen,

Catalog No. 15628-050) was used as a size standard. The results are depicted in FIG. 3.

Example 2

Demonstration of the reproducibility and specificity of a coupled one-stage process of poly-(A)-polymerase reaction and reverse transcription in the same reaction vessel

In this experiment, the feasibility of a coupled one-stage process of poly-(A)-polymerase reaction and reverse transcription should be reproduced in the same reaction vessel. For this purpose, the efficiency of the one-stage process of the poly-(A)-polymerase reaction and reverse transcription in the same reaction vessel was analyzed in the example of the detection of a 22-mer RNA oligonucleotide. A reverse transcription reaction for the template that is used according to standard conditions was used as a control for the specificity of the detection.

For this purpose, the coupled one-stage process was performed under various conditions. The latter were, on the one hand, the buffer supplied with poly-(A)-polymerase, and, on the other hand, the buffer supplied with the reverse transcriptase (Tables 7, 8).

TABLE 7 Designation and Components of the Reactions Conducted Designation Buffer Template Reaction 1 1-Step Process RNA 50 ng + mleu7a 2 × 10E9 Copies Reaction 2 in PAP Buffer RNA, 50 ng Reaction 3 Negative Control: H₂0 Reaction 4 1-Step Process RNA 50 ng + mleu7a 2 × 10E9 Copies Reaction 5 in RT Buffer RNA, 50 ng Reaction 6 Negative Control: H20 Reaction 7 Standard RT RNa 50 ng + mleu7a 2 × 10E9 Copies Reaction 8 RNA, 50 ng

TABLE 8 Table 8: Composition of the Combined Poly-(A)-Polymerase/Reverse Transcription Reaction and the Standard Reverse Transcription Reaction Composition of the Combined Poly-(A)-Polymerase/Reverse Transcription Reaction and the Standard Reverse Transcription Reaction Data from the Final Concentrations Reactions Reactions Reactions 1, 2, 3 4, 5, 6 7, 8 Reagents PAP Buffer RT Buffer Standard RT 5x PAP Buffer 1x 10x RT Buffer 1x 1x MnCl₂, 25 mmol 2.5 mmol rATP, 10 mmol 1 mmol 1 mmol Poly-(A)-Polymerase, 2 U/μl 2 U 2 U (0.1 U/μl) (0.1 U/μl) dNTP Mix (dA, dT, dG, dC, 0.5 mmol 0.5 mmol 0.5 mmol 5 mmol each) UniGAPdT Primer, 10 μmol 1 μmol 1 μmol 1 μmol RNase Inhibitor, 10 U/μl 10 U 10 U 10 U Sensiscript Reverse 1 μl 1 μl 1 μl Transcriptase RNase-Free Water Variable Variable Variable mleu7a; Reactions 1, 4, 7 2 × 10E9 2 × 10E9 2 × 10E9 Copies Copies Copies RNA: Reactions 1, 2, 4, 5, 50 ng 50 ng 50 ng 7, 8 Neg. Control (H₂O instead of H₂O H₂O RNA) in Reactions 3, 6 Total Volume 20 μl 20 μl 20 μl Incubation 1 Hour, 37° C. 5 Minutes, 93° C. All reaction batches were then divided: Batches a) 10 μl was removed and stored at 4° C.; For all batches b): Uni GAP dT primer [1 μmol] and 0.5 μl of Sensiscript Reverse Transcriptase were added again to 10 μl, and a reverse transcription was performed again (for 1 hour at 37° C.), then the reverse transcriptase was inactivated (5 minutes, 93° C.).

In addition, a standard reverse transcription reaction was performed with the purpose of examining the specificity of the detection in the subsequent PCR (Tables 7, 8, see above). After the poly-(A)-polymerase reaction and reverse transcription, the samples were divided. In each case, Uni Gap dT primer and reverse transcriptase were added again to half of a sample (see Table 7, above). The purpose here was to rule out the possibility that false-positive signals are produced to a small extent by an undesired adherence of an A-Tail to the Uni Gap dT primer. As a template, total-RNA was added, which was isolated from human blood with an RNeasy Midi Kit (QIAGEN, Hilden, Germany, Cat. No. 75144).

The components that are used in the individual reactions and their designations are put together in Table 7, see above. The detected 22-mer RNA corresponds in the sequence thereof to the human leu7a miRNA (EMBL Ace #: AJ421724) and may be expressed in human blood cells such as leukocytes. However, such small RNAs are only very inefficiently purified because of the purification technology of the RNeasy process that is used for the RNA isolation. The RNeasy process ensures only an efficient binding of RNAs with a size above 200 bases on the silica membrane of the RNeasy column (QIAGEN RNeasy Midi/Maxi Handbook, June 2001, p. 9), and thus small RNAs such as miRNAs are stripped out to a large extent.

In addition, the synthetic 22-mer RNA was used at a concentration that is clearly higher than the endogenic copy number expected. The reactions were put together as indicated in Table 8 (see above).

To this end, the reagents indicated in Table 9 were used.

TABLE 9 Materials for the Poly-A-Reaction and Reverse Transcription Poly (A) Polymerase Ambion; Material Number 80 U: 2030 Sensiscript RT Kit Qiagen; Material Number 50rxn: 205211 Adenosine 5′-Triphosphate (rATP) Amersham; Material Number 25 μmol: 27-2056-01 RNase Inhibitor Promega; Material Number: N2511 Uni GAP dT Primer 5′-TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CCT TTT TTT TTT TTT TTT TTT TTY V(N-Q)-3′ (SEQ ID NO: 2) RNA RNA Leukocytes from Human Blood Isolated with an RNeasy Midi Kit (QIAGEN, Cat. No. 75144) mleu7a RNA Oligonucleotide 5′-UGA GGU AGU AGG UUG UAU AGU U-3′ (SEQ ID NO: 1)

After the inactivation of the enzymes (5 minutes at 93° C.), the batches were diluted 1:2 with water, and 2 μl each of the batches 1a/b to 8a/b was used as a template in a real-time SYBR Green PCR. The preparation of the real-time PCR was carried out in two-fold batches as indicated in Table 9 (above) with QuantiTect SYBR Green PCR Kit (Catalog No. 204143) and the primers indicated in Table 10.

TABLE 10 Components for SYBR Green Real-Time PCR Final Concentration 2x SYBR Green PCR Master Mix 1x Hum Uni Primer, 10 μmol 0.5 μmol miRNA Primer let 7short, 10, μmol 0.5 μmol RNase-Free Water Variable PAP-/RT-Reaction 1:2 prediluted 2 μl Final Reaction Volume 20 μl

The sequence 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO: 3) contained in the universal tail-primer Hum Uni Primer was described in US 2003/0186288A 1. The PCR protocol consisted of an initial reactivation of the HotStarTaq Polymerase contained in the QuantiTect SYBR Green PCR Master Mix for 15 minutes at 95° C., followed by 40 cycles for 15 seconds at 94° C., 30 seconds at 52° C., and 30 seconds at 72° C. (see Table 11).

TABLE 11 Materials for the SYBR Green PCR QuantiTect SYBR Qiagen; Material Number: 204143 Green PCR Kit (200) let 7short 5′-GAG GTA GTA GGT TGT ATA G-3′ (Specific miRNA (SEQ ID NO: 4) Primer) Hum Uni Primer 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO: 3)

The acquisition of the fluorescence data was carried out during the 72° C. extension step. The PCR analyses were performed with an Applied Biosystems 7500 Fast Real-Time PCR System (Applied Biosystems) in a reaction volume of 20 μl and then a melt curve analysis was performed.

The coupled one-stage poly-(A)-reaction and reverse transcription are possible both in poly-(A)-polymerase buffer and in RT buffer, which is evident based on real-time PCR analyses. Preferred buffer conditions were already indicated in the text (see above). They show large differences in the Ct values that are obtained when using the different buffers.

The standard reverse transcription reactions (reactions 3, 6), performed for the monitoring of the specificity, are all negative (no Ct) without poly-(A)-reactions. This allows the conclusion that without polyadenylation of the 22-mer RNA (1, 4, 7) or the naturally occurring miRNA (2, 5, 8) as expected, no template for a PCR amplification is present and therefore no signal can be generated (“no Ct”).

In the “RT doubled” batches, additional RT enzymes and Uni Gap dT Primer were added after the first incubation with the purpose of making poly-(A)-tailed UniGap dT Primer detectable by an RT reaction, possibly in the first reaction. All of these batches showed no Ct, i.e., undesirable artifacts are not detectable.

Undesirable artifacts such as poly-(A)-tailing of the primer used for the cDNA synthesis are also not detectable.

Example 3

Detection of various miRNAs using the process according to the invention.

In this experiment, it should be demonstrated that several targets can be detected by miRNA-specific PCR Primers from a cDNA template that was synthesized with the process according to the invention with poly-(A)-reactions of common reverse transcription. For this purpose, a process was performed with 293 RNA as a template. A reverse transcription reaction for the template that is used according to standard conditions was used as a control for the specificity of the detection.

In the subsequent SYBR Green PCR, overall in each case one of 4 different specific primers for miRNAs together with the tail of specific primers was used. In addition, a primer located on the 3′-end of the human B-actin transcript was used together with a tail-specific primer to examine the efficiency of the poly-A-reaction and reverse transcription.

For the poly-A-reaction and reverse transcription (PAP+RT reaction), the reagents from Table 13 were pipetted together as indicated in Table 16.

TABLE 13 Materials for the Poly A Reaction and Reverse Transcription Poly (A) Polymerase Ambion; Material Number 80 U: 2030 Sensiscript RT Kit Qiagen; Material Number 50rxn: 205211 Adenosine 5′- Amersham; Material Number 25 μmol: 27- Triphosphate (rATP) 2056-01 RNase Inhibitor Promega; Material Number: N2511 Uni GAP dT Primer 5′-TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CCT TTT TTT TTT TTT TTT TTT TTY VN-3′ (SEQ ID NO: 2) 293 RNA: From Human Cell Line 293 (ATCC Number: CRL-1573) With Qiagen RNeasy Midi Kit Isolated

TABLE 16 PAP + RT Reaction Final Reagents Concentration 1Ox Buffer RT 1x rATP, 10 mmol 1 mmol Poly A Polymerase 2 U/μl 2 U dNTP Mix (ATGC, 5 mmol each) 0.5 mmol Uni GAP dT Primer, 10 μmol 1 μmol RNase Inhibitor, 10 U/μl 10 U Sensiscript Reverse Transcriptase 1 μl RNase-Free Water Variable a) 293 RNA, 20 ng/μl 5 μl (100 ng) b) H₂0 for Neg Control 5 μl Total Volume 20 μl Incubation 1 Hour, 37° C. 5 Minutes, 93° C.

In reaction a), 293 RNA was added as a negative control (neg control) and in reaction b), water was added as a negative control. As a control for the specificity of the detection, a standard reverse transcription reaction with the reagents indicated in Table 14 was prepared based on the diagram in Table 17.

TABLE 14 Materials for Reverse Transcription Sensiscript Qiagen; Material Number 50rxn: 205211 RT Kit RNase Promega; Material Number: N2511 Inhibitor Uni GAP 5′-TGG AAC GAG ACG ACG ACA GAC dT Primer CAA GCT TCC CGT TCT CAG CCT TTT TTT TTT TTT TTT TTT TTY VN-3′ (SEQ ID NO: 2) 293 RNA With Qiagen RNeasy Midi Kit Isolated

TABLE 17 Standard RT Reaction Reagents 2.) RT Reaction 1Ox Buffer RT 1x dNTP Mix (ATGC, 5 mmol each) 0.5 mmol Uni GAP dT Primer, 10 μmol 1 μmol RNase Inhibitor, 10 U/μl 10 U Sensiscript Reverse Transcriptase 1 μl RNase-Free Water Variable c) 293 RNA, 20 ng/μl 5 μl (100 ng) d) H₂0 for Neg Control 5 μl Total Volume 20 μl Incubation 1 Hour, 37° C. 5 Minutes, 93° C.

In reaction c), 293 RNA was added as negative control (neg control), and in reaction d), water was added as negative control. The samples were then incubated for one hour at 37° C. To stop the reaction, the reactions were incubated for 5 minutes at 93° C.; the enzymes are inactivated by this temperature step.

After the inactivation of the enzymes, the batches 1:2 were diluted with water and 2 μl each of the batches a) to d) were used as templates in a real-time SYBR Green PCR. The materials for the PCR are indicated in Table 15.

TABLE 15 Materials for the SYBR Green PCR QuantiTect SYBR Green PCR Kit (200) Qiagen; Material Number: 204143 let 7short (Specific miRNA Primer) 5′-GAG GTA GTA GGT TGT ATA G-3′ (SEQ ID NO: 4) hsa-miR-24 (Specific miRNA Primer) 5′-TGG CTC AGT TCA GCA GGA-3′ (SEQ ID NO: 5) hsa-miR-15a (Specific miRNA Primer) 5′-TAG CAG CAC ATA ATG GTT T-3′ (SEQ ID NO: 6) hsa-miR-16 (Specific miRNA Primer) 5′-TAG CAG CAC GTA AAT ATT G-3′ (SEQ ID NO: 7) B-Actin 3′ Primer 5′-GTA CAC TGA CTT GAG ACC AGT TGA ATA AA-3′ (SEQ ID NO: 8) Hum Uni Primer 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO: 3)

Ten different reaction batches were pipetted. In reactions 1-5 (Table 18), in each case the miRNA-specific or B-actin 3′ primer and the tail primer (Hum Uni) were used.

TABLE 18 SYBR GREEN PCR Reactions 1-5 Final Components for SYBR Green PCR Concentration 2x SYBR Green PCR Master Mix 1x Hum Uni Primer, 10 μmol 0.5 μmol One Specific miRNA Primer Each (10 μmol) 0.5 μmol let 7short hsa-miR-24 hsa-miR-15a hsa-miR-16 RNase-Free Water Variable PAP + RT Reaction a) b) 1:2 prediluted 2 μl (5 ng) Standard RT Reaction c) d) 1:2 prediluted 2 μl (5 ng) or H₂0 as Neg Control 2 μl Final Reaction Volume 20 μl

In reactions 6-10 (Table 19), in each case only one primer was used, either the miRNA specific primer or the tail-specific primer.

In reactions 6-10 (Table 19), in each case only one primer was used, either the miRNA specific primer or the tail-specific primer.

TABLE 19 Control with Only One Primer Reaction 6-10 Final Components for SYBR Green PCR Concentration 2x SYBR Green PCR Master Mix 1x One Specific miRNA Primer Each (10 μmol) 0.5 μmol let 7short hsa-miR-24 hsa-miR-15a hsa-miR-16 Each with 3′ Hum Uni Primer RNase-Free Water Variable PAP + RT Reaction a) b) 1:2 Prediluted 2 μl (5 ng) Standard RT Reaction c) d) 1:2 Prediluted 2 μl (5 ng) or H₂0 as Neg Control 2 μl Final Reaction Volume 20 μl

The sequence in which the primers were used in the reactions can be seen from Table 20. The preparation of the real-time PCR was carried out in two-fold batches.

TABLE 20 Primer Primer Reaction 1 β-Actin 3′Primer + Hum Uni Reaction 2 let 7short + Hum Uni Reaction 3 hsa-miR-24 + Hum Uni Reaction 4 hsa-miR-15a + Hum Uni Reaction 5 hsa-miR-16 + Hum Uni Reaction 6 Hum Uni Reaction 7 let 7short Reaction 8 hsa-miR-24 Reaction 9 hsa-miR-15a Reaction 10 hsa-miR-16

The sequence AAC GAG ACG ACG ACA GAC (SEQ ID NO: 3) contained in the universal Tail-Primer Hum Uni Primer was described in US2003/0186288A 1.

The PCR protocol consisted of an initial reactivation of the HotStarTaq polymerase contained in the QuantiTect SYBR Green PCR Master Mix for 15 minutes at 95° C., followed by 40 cycles for 15 seconds at 94° C., 30 seconds at 52° C., and 30 seconds at 72° C. (see Table 21). The acquisition of the fluorescence data was carried out during the 72° C. extension step. The PCR analyses were performed with an Applied Biosystems 7000 Fast Real-Time PCR System (Applied Biosystems) in a reaction volume of 20 μl, and then a melt curve analysis was performed.

TABLE 21 3-Step PCR Protocol PCR Initial Reactivation 15 Minutes, 95° C. Denaturation 15 Seconds, 94° C. 40x Annealing 30 Seconds, 52° C. Extension 30 Seconds, 72° C. Melt Curve

It is shown that the efficiency of the reverse transcription performed under standard conditions and of the process according to the invention for the B-actin system that is selected by way of example is comparable, which is evident in comparable Ct values in the real-time PCR (FIG. 6).

When using the cDNA produced under standard conditions, the real-time PCR yields very high Ct values of above 38, which mean a very good specificity of the detection in a real-time PCR that is performed with SybrGreen (FIG. 6). In the agarose gel analysis of the PCR products, PCR products of the expected values were detected (FIG. 8), or no product was detected when using the cDNA produced under standard conditions.

The miR24 product represents an acquisition. Here, when the cDNA produced under standard conditions is used, a PCR product of the wrong size is produced (FIG. 8, see also FIG. 6). This product cannot be detected, as soon as a cDNA is used, which was produced using the process according to the invention (FIG. 8).

All control reactions in which water instead of RNA template was used in the reverse transcription or the process according to the invention show no signal, i.e., no Ct value in the real-time PCRs in question was obtained (FIG. 7, upper part). The same also applies for reactions in which only one primer was used (FIG. 7, upper part). Also, no Ct value was obtained for negative controls, in which water instead of cDNA was used in the PCR (FIG. 7).

Example 4

Detection of miRNA using the coupled, one-stage process of poly-A-reaction and reverse transcription and subsequent detection of the generated cDNA over real-time PCR with a tail-specific probe.

In this experiment, a real-time PCR was performed, in which a Taqman probe was used, which has a specific binding site on the tail-primer (Uni Gap dT). The detection via a probe represents a conceivable alternative for the detection via SYBR Green real-time PCR. The use of the probe offers the additional possibility of a multiplex PCR, i.e., a co-amplification or one or more additional target nucleic acids, such as an internal control, which can be, e.g., a housekeeping gene.

For the poly-A-reaction and reverse transcription (PAP+RT reaction), the reagents from Table 22 were pipetted together as indicated in Table 24.

TABLE 22 Materials for the Poly A Reaction and Reverse Transcription Poly (A) Polymerase Ambion; Material Number 80 U: 2030 Sensiscript RT Kit Qiagen; Material Number 50rxn: 205211 Adenosine Amersham; Material Number 25 μmol: 27- 5′-Triphosphate (rATP) 2056-01 RNase Inhibitor Promega; Material Number; N2511 Uni GAP dT Primer 5′-TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CCT TTT TTT TTT TTT TTT TTT TTY VN-3′ (SEQ ID NO: 2) mleu7a Oligonucleotide 5′-VGA GGU AGU AGG UUG UAU AGU U-3′ (SEQ ID NO: 1)

TABLE 24 PAP + RT Reaction Final Reagents Concentration 10x Buffer RT 1x rATP, 10 mmol 1 mmol Poly A Polymerase, 2 U/μl 2 U dNTP Mix (ATGC, 5 mmol each) 0.5 mmol Uni GAP dT Primer, 10 μmol 1 μmol RNase Inhibitor, 10 U/μl 10 U Sensiscript Reverse Transcriptase 1 μl RNase-Free Water Variable mleu7 (10″9 Copies/μl) 2 μl (2 × 10″9 Copies) Total Volume 20 μl Incubation 1 Hour, 37° C. 5 Minutes, 93° C.

Then, the reaction batch was incubated at 37° C., followed by an inactivation of the enzymes for 5 minutes to 93° C.

After the inactivation of the enzymes, 2 μl of the undiluted batch was used as a template in a real-time PCR, which contained a Taqman probe for detection. The materials for the PCR are indicated in Table 23 and were pipetted together as indicated in Table 25.

TABLE 23 Materials for the QT Probe PCR QuantiTect Probe Qiagn Material No.: 204343 PCR Kit (200) let 7short 5′-GAG GTA GTA GGT TGT ATA G-3′ (Specific miRNA (SEQ ID NO: 4) primer) Hum Uni Primer 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO: 3) Hum Uni Probe 5′-HEX-CAA GCT TCC CGT TCT CAG CC-BHQ-3′ (SEQ ID NO: 9) 5′ Reporter Dye: HEX 3′ Quencher: Black Hole Quencher 1

TABLE 25 QuantiTect Probe PCR Final Components for QuantiTect Probe PCR Concentration 2x QuantiTect Probe PCR Master Mix 1x Hum Uni Primer, 10 μmol 0.5 μmol let 7short (specific miRNA Primer) 0.5 μmol RNase-Free Water Variable PAP + RT Reaction, Undiluted 2 μl (2 × 10″8 Copies) Final Reaction Volume 20 μl

The batch of real-time PCR was carried out in two-fold batches.

The sequence AAC GAG ACG ACG ACA GAC (SEQ ID NO: 3) contained in the universal tail-primer Hum Uni Primer was described in US2003/0186288A 1. The Taqman probe sequence was removed in the human GAPDH gene locus; it is not contained in US2003/0186288A 1.

The PCR protocol consisted of an initial reactivation of the HotStarTaq polymerase contained in the QuantiTect Probe PCR Master Mix for 15 minutes at 95° C., followed by 45 cycles for 15 seconds at 94° C. and 30 seconds at 52° C. (see Table 26).

TABLE 26 2-Step PCR Protocol PCR Initial Reactivation 15 Minutes, 95° C. Denaturation 15 Seconds, 94° C. 45x Annealing 30 Seconds, 52° C.

The acquisition of the fluorescence data was carried out during the 52° C. annealing step. The PCR analyses were performed with a 7700 sequence detection system (Applied Biosystems) in a reaction volume of 20 μl. The PCR results are shown in Table 27.

TABLE 27 PCR Results mleu7a Ct Ct Agent CV in % Undiluted, 2 × 10″8 20.24 20.31 0.45 20.37

A detection using a tail-specific probe is possible and yields the expected result.

Example 5

Effect of poly-A-polymerase concentration and incubation time in the coupled, one-stage process of poly-A-reaction and reverse transcription.

In this test, two concentrations of poly-A-polymerase (2 U or 0.5 U) were used for 15 minutes or 1 hour respectively in the process according to the invention. All conditions were tested in each case in the RT buffer (Qiagen) and poly-A-polymerase buffer.

For the poly-A-reaction and reverse transcription (PAP+RT reaction), the reagents from Table 28 were pipetted together as indicated in Table 30: reaction a) 2 U of poly-A-polymerase, reaction b) 0.5 U of poly-A-polymerase).

TABLE 28 Materials for the Poly A Reaction and Reverse Transcription Poly (A) Polymerase Ambion; Material Number 80 U: 2030 Sensiscript RT Kit Qiagen; Material Number 50rxn: 205211 Adenosine Amersham; Material Number, 25 μmol: 27- 5′-Triphosphate (rATP) 2056-01 RNase Inhibitor Promega; Material Number: N2511 Uni GAP dT Primer 5′-TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CCT TTT TTT TTT TTT TTT TTT TTY VN-3′ (SEQ ID NO: 2) Corn RNA From 1 g of Ground Corn Husks with Qiagen RNeasy Mini Kit (Cat. No. 74106) according to Plant Protocol. mleu7a Oligonucleotide 5′-VGA GGU AGU AGG UUG UAU AGU U-3′ (SEQ ID NO: 1)

TABLE 30 PAP + RT Reaction Final Reagents Concentration 10x Buffer RT 1x rATP, 10 mmol 1 mmol Poly A Polymerase, 2 U/μl a) 2 U b) 0.5 U dNTP Mix (ATGC, 5 mmol each) 0.5 mmol Uni GAP dT Primer, 10 μmol 1 μmol RNase Inhibitor, 10 U/μl 10 U Sensiscript Reverse Transcriptase 1 μl RNase-Free Water Variable mleu7 a 10″9 Copies/μl 2 μl (2 × 10″9 Copies) Corn RNA, 25 ng/μl 2 μl (50 ng) Total Volume 20 μl 1.) Incubation 1 Hour, 37° C. 5 Minutes, 93° C. 2.) Incubation 15 Minutes, 37° C.  5 Minutes, 93° C.

Then, the samples were incubated at 37° C. (1. 1 hour/2. 15 minutes). Then, the reactions were heated for 5 minutes to 93° C., and thus the enzymes were inactivated.

Then, in each case 2 μl was incorporated undiluted into an SYBR Green PCR for each reaction. The reactions were tested two times apiece. For this purpose, the reagents from Table 29 were pipetted together as indicated in Table 31, and then the PCR was performed as indicated in Table 32.

TABLE 29 Materials for the SYBR Green PCR QuantiTect SYBR Qiagen; Material Number: 204143 Green PCR Kit (200) let 7short 5′-GAG GTA GTA GGT TGT ATA G-3′ (Specific miRNA (SEQ ID NO: 4) Primer) Hum Uni Primer 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO: 3)

TABLE 31 SYBR GREEN PCR Final Components for SYBR Green PCR Concentration 2x SYBR Green PCR Master Mix 1x Hum Uni Primer, 10 μmol 0.5 μmol let 7short (Specific miRNA Primer) 0.5 μmol RNase-Free Water Variable PAP + RT Reaction 1a) b)/2a) b) 2 μl (2 × 10″8 Copies) Final Reaction Volume 20 μl

TABLE 32 3-Step PCR Protocol PCR Initial Reactivation 15 Minutes, 95° C. Denaturation 15 Seconds, 94° C. 45x Annealing 30 Seconds, 52° C. Extension 30 Seconds, 70° C. Melt Curve

The PCR protocol consisted of an initial reactivation of the HotStarTaq polymerase contained in the QuantiTect SYBR Green PCR Master Mix for 15 minutes at 95° C., followed by 40 cycles for 15 seconds at 94° C., 30 seconds at 52° C., and 30 seconds at 72° C. (see Table 32 above). The acquisition of the fluorescence data was carried out during the 72° C. extension step. The PCR analyses were performed with an Applied Biosystems 7000 Real-Time PCR System (Applied Biosystems) in a reaction volume of 20 μl, and then a melt curve analysis was performed.

A dependency of the efficiency of the one-stage process of the poly-A-reaction and reverse transcription both on the concentration of the poly-A-polymerase and on the incubation time can be seen (see FIG. 9).

Example 6

Implementation of the process according to the invention with various reverse transcriptases.

The process according to the invention was applied with a total of five different reverse transcriptases (see Table 35) in the buffer RT (Qiagen) (reactions 1-5) and additionally, for purposes of comparison, in each case in the buffer supplied with the reverse transcriptase (reactions 6-9).

TABLE 35 Reverse Transcriptases and Buffers that are Used 1.) AMV Reverse Transcriptase AMV Reverse Transcriptase 5 x 2.) SuperScript III Reverse Reaction Buffer Transcriptase 5 x First-Strand Buffer 3.) HIV Reverse Transcriptase 10 x First-Strand Synthesis Buffer 4.) M-MuLV Reverse Transcriptase 10 x Reverse Transcriptase 5.) Sensiscript Reverse Reaction Buffer Transcriptase 10 x Buffer RT

For the one-stage process of poly-A-reaction and reverse transcription (PAP+RT reaction), the reagents from Table 33 were pipetted together for reactions 1-5 (reaction buffer: buffer RT (Qiagen) as indicated in Table 36 and for reactions 6-9 (additional reverse transcriptases, in each case in the buffer that is supplied) as indicated in Table 37.

TABLE 33 Materials for the Poly A Reaction and Reverse Transcription Poly (A) Polymerase Ambion; Material Number 80 U: 2030 AMY Reverse Transcriptase Promega; Material Number 300 U: M5101 SuperScript III Reverse Transcriptase Invitrogen; Material Number 10,000 U: 18080-044 HIV Reverse Transcriptase Ambion; Material Number 500 U: #2045 M-MuLV Reverse Transcriptase BioLabs; Material Number 10,000 U: M0253S Sensiscript RT Kit Qiagen; Material Number 50 rxns: 205211 Adenosine 5′-Triphosphate (rATP) Amersham; Material Number 25 μmol: 27- 2056-01 RNase Inhibitor Promega; Material Number: N2511 Uni GAP dT Primer 5′-TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CCT TTT TTT TTT TTT TTT TTT TTY V-3′ (SEQ ID NO: 2) Corn RNA From 1 g of Ground Corn Husks with Qiagen RNeasy Mini Kit (Cat. No. 74106) Plant Protocol, 10-Fold Upscale (Maxi Shredder and Column) mleu7a Oligonucleotide 5′-VGA GGU AGU AGG UUG UAU AGU U-3′ (SEQ ID NO: 1)

TABLE 36 PAP + RT Reaction in Buffer RT (Qiagen) Final Reagents Concentration 10x Buffer RT 1x rATP, 10 mmol 1 mmol Poly A Polymerase, 2 U/μl 1 U dNTP Mix (ATGC, 5 mmol each) 0.5 mmol Uni GAP dT Primer, 10 μmol 1 μmol RNase Inhibitor 10 U/μl 10 U 1.) AMV Reverse Transcriptase 24 U 2.) SuperScript III Reverse Transcriptase 10 U 3.) HIV Reverse Transcriptase 1 U 4.) M-MuLV Reverse Transcriptase 10 U 5.) Sensiscript Reverse Transcriptase 1 μl RNase-Free Water Variable Mleu7 a 10″9 Copies/μl 2 μl (2 × 10″9 Copies) Corn RNA, 20 ng/μl 2 μl (40 ng) Total Volume 20 μl Incubation 1 Hour, 37° C. 5 Minutes, 93° C.

TABLE 37 PAP + RT Reaction in Buffer Supplied with the Reverse Transcriptase Final Reagents Concentration 6.) AMV Reverse Transcriptase 5 x Reaction Buffer 1x 7.) 5 x First-Strand Buffer 1x 8.) 10 x First-Strand Synthesis Buffer 1x 9.) 10 x Reverse Transcriptase Reaction Buffer 1x rATP, 10 mmol 1 mmol Poly A Polymerase, 2 U/μl 1 U dNTP Mix (ATGC, 5 mmol each) 0.5 mmol Uni GAP dT Primer, 10 μmol 1 μmol RNase Inhibitor, 10 U/μl 10 U 6.) AMV Reverse Transcriptase 24 u 7.) 7.) SuperScript III Reverse Transcriptase 10 U 8.) HIV Reverse Transcriptase 1 U 9.) M-MuLV Reverse Transcriptase 10 U RNase-Free Water Variable mleu7 a 10″9 Copies/μl 2 μl (2 × 10″9 Copies) Corn RNA, 20 ng/μl 2 μl (40 ng) Total Volume 20 μl Incubation 1 Hour, 37° C. 5 Minutes, 93° C.

Then, the samples were incubated for 1 hour at 37° C. Then, the reactions were heated for 5 minutes to 93° C., and thus the enzymes were inactivated.

Subsequently, in each case 2 μl was incorporated into an SYBR Green PCR for each reaction. The reactions were tested two times apiece. For this purpose, the reagents from Table 34 were pipetted together as indicated in Table 38, and the PCR was performed as indicated in Table 39.

TABLE 34 Materials for the SYBR Green PCR QuantiTect SYBR Qiagen; Material Number: 204143 Green PCR Kit (200) Let 7short 5′-GAG GTA GTA GGT TGT ATA (Specific miRNA G-3′ (SEQ ID NO: 4) Primer) Hum Uni Primer 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO: 3)

TABLE 38 SYBR GREEN PCR Final Components for SYBR Green PCR Concentration 2x SYBR Green PCR Master Mix 1x Hum Uni Primer, 10 μmol 0.5 μmol let 7short (Specific miRNA Primer) 0.5 μmol RNase-Free Water Variable PAP + RT Reaction, Undiluted 2 μl (2 × 10{circumflex over ( )}8 Copies) Final Reaction Volume 20 μl

TABLE 39 3-Step PCR Protocol PCR Initial Reactivation 15 Minutes, 95° C. Denaturation 15 Seconds, 94° C. 45x Annealing 30 Seconds, 52° C. Extension 30 Seconds, 70° C. Melt Curve

The PCR protocol consisted of an initial reactivation of the HotStarTaq polymerase contained in the QuantiTect SYBR Green PCR Master Mix for 15 minutes at 95° C., followed by 40 cycles for 15 seconds at 94° C., 30 seconds at 52° C., and 30 seconds at 72° C. (see Table 39). The acquisition of the fluorescence data was carried out during the 72° C. extension step. The PCR analyses were performed with an Applied Biosystems 7000 Real-Time PCR System (Applied Biosystems) in a reaction volume of 20 μl, and then a melt curve analysis was performed.

The amounts of reverse transcriptases used were optimized for standard reverse transcription reactions, which can be a likely explanation for the differences in the Ct value that are observed.

Example 7

Demonstration of the feasibility of a coupled, three-stage process of poly-A-reaction, reverse transcription and PCR in the same reaction vessel; effect of various additions to the efficiency of the detection of a 22-mer RNA oligonucleotide.

In this experiment, the feasibility of a coupled, three-stage process of the poly-(A)-polymerase reaction, reverse transcription and PCR in the same reaction vessel should be demonstrated. For this purpose, the coupled, three-stage process was performed with the indicated batches under the following conditions.

As a control, the reaction was performed in a two-stage process based on FIG. 1 B.

For the three-stage process of poly-A-reaction, reverse transcription and PCR (PAP+RT reaction+PCR), the materials from Table 40 were put together as indicated in Table 41.

TABLE 40 Materials for the Poly A Reaction, Reverse Transcription and PCR Poly (A) Polymerase Epicenter Biotechnologies; Material Number 400 U: PAP5104 QuantiTect Multiplex RT-PCR Kit Qiagen; Material Number 200 rxns: 204643. Adenosine 5′-Triphosphate (rATP) Amersham; Material Number, 25 μmol: 27- 2056-01 dNTP Mix (ATGC, 10 mmol each) Amersham; Material Number Qiagen Intern 1007430 RNase Inhibitor Promega; Material Number: N2511 Uni GAP dT Primer 5′-TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CCT TTT TTT TTT TTT TTT TTT TTY VN-3′ (SEQ ID NO: 2) Com RNA From 1 g of Ground Com Husks with Qiagen RNeasy Mini Kit (Cat. No. 74106) Plant Protocol, 10-Fold Upscale (Maxi Shredder and Column) See Above mleu7a Oligonucleotide 5′-VGA GGU AGU AGG UUG UAU AGU U-3′ (SEQ ID NO: 2) let 7short (Specific miRNA Primer) 5′-GAG GTA GTA GGT TGT ATA G-3′ (SEQ ID NO: 1) Hum Uni Primer 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO: 4) GAPDH-TM-HEX_BHQ 5′HEX-CAA GCT TCC CGT TCT CAG Poly A RNA CC-BHQ 3′ (SEQ ID NO: 3) Amersham Random N8 Primer Biosciences Material Number 27-4110-01, Oligo dT 12 Dissolved with 25 μg/μl in RNase-Free Water NNNNNNNN TTTTTTTTTTTT-3′ (SEQ ID NO: 20) Phosphate

TABLE 41 PAP + RT Reaction + PCR with Batches in QuantiTect Multiplex RT- PCR Master Mix (Qiagen) Final Reagents Concentration 2x QuantiTect Multiplex RT-PCR Master Mix 1 x rATP, 10 mmol 100 μmol Poly A Polymerase, 4 U/μl 1 U dNTP Mix (ATGC, 10 mmol each) 0.5 mmol Uni GAP dT Primer, 10 μmol 0.05 μmol RNase Inhibitor, 40 U/μl 10 U QuantiTect Multiplex RT Mix 0.2 μl Hum Uni Primer, 10 μmol 0.5 μmol let 7short (Specific miRNA Primer) 0.5 μmol GAPDH-TM-HEX_BHQ 0.2 μmol RNase-Free Water Variable Poly A RNA, 25 μg/μl 10 ng/μl N8 Random Primer 0.05 μmol Oligo dT12 5 μmol mleu7 a 10″9 Copies/μl 2 μl (2 × 10⁹ Copies) Corn RNA, 20 ng/μl 2 μl (40 ng) Total Volume 20 μl

The reactions were tested three times apiece. For this purpose, the reagents from Table 40 were pipetted together as indicated in Table 41, and the reaction was performed as indicated in Table 42.

TABLE 42 Reaction Protocol of the “3-in-1” Reaction Poly A Reaction and 45 Minutes, 37° C. Reverse Transcription 15 Minutes, 50° C. PCR Initial Reactivation 15 Minutes, 95° C. Denaturation 15 Seconds, 94° C. 45x Annealing/Extension 30 Seconds, 52° C.

The reaction protocol first consisted of conditions for the combined reaction of poly-A polymerase and reverse transcription with the QuantiTect Multiplex Reverse Transcriptase Mix (45 minutes, 37° C., and 15 minutes, 50° C.). From this followed an incubation for 15 minutes at 95° C., with the purpose of inactivating the poly-A-polymerase and reverse transcriptase and activating the HotStarTaq DNA polymerase that is contained in the QuantiTect Multiplex RT-PCR Master Mix. 45 PCR cycles followed for 15 seconds at 94° C. and for 30 seconds at 52° C. (see Table 43) to amplify the generated let7a-cDNA in a real-time PCR. For detection, a fluorescence-labeled probe specific to the 5′-tail of the Uni Gap dT primer was used. The acquisition of the fluorescence data was carried out during the 52° C. annealing/extension step. The “3-in-1” reaction was performed with an Applied Biosystems 7500 Fast Real-Time PCR System (Applied Biosystems) in a reaction volume of 20 μl.

As shown in FIG. 14, the “3-in-1” reaction allows the specific detection of the synthetic 22mer RNA oligonucleotide in the background of com RNA. The sample, which contains the synthetic 22mer RNA oligonucleotide in the background of com RNA, supplies a Ct value of 20.61, whereby the control reaction with com RNA yielded a Ct value of 309.65. This experiment shows that the “3-in-1” reaction can technically be used under the given conditions.

Example 8

Implementation of the “3-in-1” process according to the invention with use of a manual PCR primer “Hot Starts,” with the purpose of promoting the reaction of the coupled, three-stage process. As a control, the reaction was performed in a two-stage process based on FIG. 1 B.

The reactions were put together with the materials indicated in Table 43 as indicated in Table 44.

TABLE 43 Materials for the Poly A Reaction, Reverse Transcription and PCR Poly (A) Polymerase Epicenter Biotechnologies; Material Number 400 U: PAP5104 QuantiTect Multiplex RT-PCR Kit Qiagen; Material Number 200 rxns: 204643 Adenosine 5′-Triphosphate (rATP) Amersham; Material Number 25 μmol: 27- 2056-01 dNTP Mix (ATGC, 10 mmol each) Amersham; Material Number Qiagen Intern 1007430 RNase Inhibitor Promega; Material Number: N2511 Uni GAP dT Primer 5′-TGG AAC GAG ACG ACG ACA GAC CAA GCT TCC CGT TCT CAG CCT TTT TTT TTT TTT TTT TTT TTY VN-3′ (SEQ ID NO: 2) Com RNA From 1 g of Ground Com Husks with Qiagen RNeasy Mini Kit (Cat. No. 74106) Plant Protocol, 10-Fold Upscale (Maxi Shredder and Column) mleu7a Oligonucleotide 5′-VGA GGU AGU AGG UUG UAU AGU U-3′ (SEQ ID NO: 1) PCR Primer: let 7short (Specific miRNA Primer) 5′-GAG GTA GTA GGT TGT ATA G-3′ (SEQ ID NO: 4) Hum Uni Primer 5′-AAC GAG ACG ACG ACA GAC-3′ (SEQ ID NO: 3) GAPDH-TM-HEX_BHQ Amersham Biosciences Material Number 27- Additions: 4110-01, Dissolved with 25 μg/μl in RNase- Poly A RNA Free Water Random N8 Primer NNNNNNNN Oligo dT 12 TTTTTTTTTTTT-3′ (SEQ ID NO: 2) Phosphate

TABLE 44 PAP + RT Reaction + PCR in QuantiTect Multiplex RT-PCR Master Mix (Qiagen) Final Reagents Concentration 2x QuantiTect Multiplex RT-PCR Master Mix 1 x rATP, 10 mmol 100 μmol Poly A Polymerase, 4 U/μl 1 U dNTP Mix (ATGC, 5 mmol each) 0.5 mmol Uni GAP dT Primer, 10 μmol 0.05 μmol RNase Inhibitor, 40 U/μl 10 U QuantiTect Multiplex RT Mix 0.2 μl RNase-Free Water Variable Poly A, 25 μg/μl 10 ng/μl N8 Random Primer 0.05 μmol Oligo dT12 5 μmol mleu7 a 10″9 Copies/μl 2 μl (2 × 10⁹ Copies) Corn RNA, 20 ng/μl 2 μl (40 ng) Total Volume 20 μl

With the PCR primers from Table 45, a primer mix is produced, and the required amount for respectively one reaction is pipetted in each case into a cover of an optical cap (covers for real-time PCR vessels, Applied Biosystems; Material Number 4323032). Then, the cover was incubated on a heating block at 37° C. for about 20 minutes until the liquid was evaporated, and thus the primer was dried.

After the complete drying of the PCR primer in the cover, the reagents are pipetted together as in Table 44 and added in Optical Tubes (real-time PCR vessels, Applied Biosystems; Material Number 4316567), sealed with the pretreated optical caps, and the PCR is performed as indicated in Table 47.

The reactions were tested three times apiece.

TABLE 45 Composition of Dried Oligo-Mix in the PCR Cover Amount of Final Concentration in Oligo/rxn PCR After the Hum Uni Primer 10 pmol 0.5 μmol let 7short (Specific miRNA 10 pmol 0.5 μmol Primer GAPDH-TM-HEX_BHQ  4 pmol 0.2 μmol

TABLE 46 Reaction Protocol of the “3-in-1” Reaction Poly A Reaction and 45 Minutes, 37° C. — Reverse Transcription 15 Minutes, 50° C. Incubation 95° C., 3 Minutes Briefly Invert 8-Strip Reaction Vessel to Dissolve the Primer, Dried in the Cover, in the Reaction Mix PCR Initial Reactivation 12 Minutes, 95° C. Denaturation 15 Seconds, 94° C. 45x Annealing/Extension 30 Seconds, 52° C.

The reaction protocol first consisted of conditions for the combined reaction of poly-A polymerase and the reverse transcription with the QuantiTect Multiplex Reverse Transcriptase Mix (45 minutes, 37° C., and 15 minutes, 50° C.). Then, the reactions were heated for 3 minutes to 95° C. with the purpose of inactivating the poly-A-polymerase and reverse transcriptase enzymes. Then, the PCR tubes were briefly removed from the device and inverted, with the purpose of redissolving the dried primer that is present in the covers and making it available for the following PCR reaction. An incubation followed from this for 12 minutes at 95° C. to activate the HotStarTaq DNA polymerase contained in the QuantiTect Multiplex RT-PCR Master Mix. A reactivation that is shorter by 3 minutes was selected here, since the reaction mix was already heated previously for inactivating the poly-A-polymerase and reverse transcriptase enzymes for 3 minutes to 95° C. 45 PCR cycles followed for 15 seconds at 94° C. and 30 seconds at 52° C. (see Table 47) to amplify the generated let7a-cDNA in a real-time PCR. For detection, a fluorescence-labeled probe specific to the 5′-tail of the Uni Gap dT Primer was used. The acquisition of the fluorescence data was carried out during the 52° C. annealing/extension step. The “3-in-1” reaction was performed with an Applied Biosystems 7500 Real-Time PCR System (Applied Biosystems) in a reaction volume of 20 μl.

FIGURES

FIG. 1A-FIG. 1B shows a comparison between the one-stage process according to this invention (B) and the two-stage process as it is known in the prior art (A). Poly A polymerase: enzyme with polyadenylenation activity in terms of the invention; reverse transcriptase: enzyme with reverse transcriptase activity in terms of the invention; rATP: ribonucleotide, here adenosine-5′-triphosphate by way of example; dNTPs: deoxyribonucleotides; oligo dT tail primer: anchor oligonucleotide with various possible embodiments in terms of the invention; Uni GAP dT primer: special embodiment of the anchor oligonucleotide; tail: 5′ tail as an optional part of the anchor oligonucleotide; w: defines the length according to the invention of the homopolymer tail that is attached by the polyadenylation activity (greater than 10-20 bases); x, y: defines the type and length according to the invention of the 3′-anchor sequence of the anchor oligonucleotide according to the invention; z: defines the length of the homopolymer portion of the anchor oligonucleotide according to the invention. FIG. 1 discloses “AAAAA[A]_(1-w),” as SEQ ID NO: 21.

FIG. 2 shows a graphic depiction of the Ct values from Table 6: Condition a) contained templates in each case, and in condition b), only H₂0, instead of templates, was added (H₂0 in PAP reaction). In b), no signal up to PCR cycle 40 (maximum number of the cycles performed) was obtained, therefore the indication is “No Ct.”

FIG. 3 shows an agarose gel analysis of the real-time PCR products from Example 1. M: 100 bp ladder (Invitrogen, Catalog No. 15628-050). 2% Agarose, colored with ethidium bromide in TAE as a running buffer. Loading diagram: Trace 1: markers, then in each case the 3× determinations have been plotted next to one another: 1a, 1b, 2a, 2b, 3a, 3b, 4a, 4b.

FIG. 4 shows a tabular depiction of Ct values that were obtained by real-time PCR analysis of the reaction products of the batches described in Table 8. At 3 and 6, no signal up to PCR cycle 40 (maximum number of the cycles performed) was obtained; therefore the indication is “no Ct.”

FIG. 5 shows a graphic depiction of Ct values that were obtained by real-time PCR analysis of the reaction products of the batches described in Table 8.

FIG. 6 shows a tabular depiction of Ct mean values that were obtained by real-time PCR analysis of the reaction products of the batches b) and e) described in Table 18.

In 2, 4 and 5 with standard RT, a signal was detected at the earliest only after cycle 38 or in 2), no signal, therefore the indication is “no Ct.”

FIG. 7 shows a tabular depiction of real-time PCR results of batches b) and d) from Table 18, as well as the controls with only one primer from Table 19, batches a)-d). No signal up to PCR cycle 40 (maximum number of the cycles performed) was obtained; therefore the indication is “no Ct.”

FIG. 8 shows an agarose gel analysis of the real-time PCR products from Example 3. M: 100 bp ladder (Invitrogen, catalog No. 15628-050). 2% Agarose, colored with ethidium bromide in TAE as a running buffer.

FIG. 9 shows a tabular depiction of Ct mean values that were obtained by real-time PCR analysis of the reaction products of the batches 1a), b) and 2a), b) described in Table 30.

Lower Part:

Graphic depiction of Ct mean values that were obtained by real-time PCR analysis of the reaction products of the batches described in Table 30.

FIG. 10 shows a tabular depiction of the Ct mean values that were obtained by real-time PCR analysis of the reaction products of the batches described in Table 36, 1-5, and in Table 37, 6-9.

Lower Part:

Graphic depiction of Ct mean values that were obtained by real-time PCR analysis of the reaction products of the batches described in Table 36, 1-5 and in Table 37, 6-9.

FIG. 11 shows a list of the nucleic acid sequences used.

FIG. 12 shows anchor oligonucleotides according to the invention. FIG. 12 discloses “poly(T)15-50” as SEQ ID NO: 22 and “Anchor Oligonucleotides” as SEQ ID Nos: 23-26, 26-27 and 10-19, respectively, in order of appearance.

FIG. 13A-FIG. 13B shows a comparison between the one-stage “3-in-1” process according to this invention (B) and the three-stage process as it is known in the prior art (A). Poly A polymerase: enzyme with polyadenylation activity in terms of the invention; (FIG. 13 discloses “AAAA[A]_(1-w),” as SEQ ID NO: 21).

Reverse transcriptase: enzyme with reverse transcriptase activity in terms of the invention;

rATP: ribonucleotide, here adenosine-5′-triphosphate by way of example;

dNTPs: deoxyribonucleotides;

Oligo dT tail primer: anchor oligonucleotide with various possible embodiments in terms of the invention;

Uni GAP dT primer: special embodiment of the anchor oligonucleotide; Tail: 5′-Tail as an optional part of the anchor oligonucleotide;

w: defines the length, according to the invention, of the homopolymer tails that are attached by the polyadenylation activity (greater than 10-20 bases);

x, y: defines the type and length, according to the invention, of the 3′-anchor sequence of the anchor oligonucleotide according to the invention;

z: defines the length of the homopolymer portion of the anchor oligonucleotide according to the invention.

PCR primer: at least one oligonucleotide for specific detection of the cDNA species, optionally at least one probe;

PCR enzyme: enzymatic activity that allows the specific detection of the cDNA species contained in the sample.

FIG. 14 shows a tabular depiction of the Ct mean values of a “3-in-1” reaction, i.e., the combined poly-(A)-polymerase reaction, reverse transcription and real-time PCR analysis coupled in a reaction vessel, according to the reaction batch from Example 7 corresponding to Table 41 and the reaction batch from Table 42.

Lower Part:

Graphic depiction of Ct mean values of a “3-in-1” reaction, i.e., the combined poly-(A)-polymerase reaction, reverse transcription and real-time PCR analysis coupled in a reaction vessel, according to the reaction batch from Example 7 corresponding to Table 41 and the reaction batch from Table 42.

FIG. 15 shows a tabular depiction of Ct mean values of a “3-in-1” reaction, i.e., the combined poly-(A)-polymerase reaction, reverse transcription and real-time PCR analysis coupled in a reaction vessel, after the reaction batch of Example 8 corresponding to Table 44 and the reaction batch from Table 46.

Lower Part:

Graphic depiction of Ct mean values of a “3-in-1” reaction, i.e., the combined poly-(A)-polymeras reaction, reverse transcription, and real-time PCR analysis coupled in a reaction vessel.

FIG. 16 shows various amounts (10 pg to 1 μg) of miRNAeasy RNA, which were reverse transcribed with use of miScript in the presence or absence of 100 ng of poly-(A) or poly-(C). The thus produced cDNA was used in a real-time PCR; in this case, miR-16 and let-7a were tested.

FIG. 17 shows various amounts (10 pg to 1 μg) of miRNAeasy RNA, which were reverse transcribed with use of miScript in the presence or absence of various amounts of poly(A). The thus produced cDNA was used in a real-time PCR; in this case, miR-16 was tested.

FIG. 18 shows various amounts (10 pg to 1 μg) of miRNAeasy RNA, which were reverse transcribed with use of miScript in the presence or absence of various amounts of poly-(C). The thus produced cDNA was used in a real-time PCR; in this case, miR-16 was tested.

FIG. 19 shows the use of 10 pg of miRNeasy RNA, which was reverse transcribed in the presence or absence of 50 ng of poly-(C) with use of the miScript RT Kit. The thus produced cDNA was used in a real-time PCR to detect GAPDH.

FIG. 20 shows various amounts (1-100 ng) of miRNeasy RNA, which were reverse transcribed with use of miScript in the presence or absence of various amounts of poly-(C). The thus produced cDNA was used in a real-time PCR, in this case to test GADPH.

FIG. 21 shows the use of 10 and 100 pg of miRNeasy RNA, which were reverse transcribed in the presence or absence of 50 ng of poly-(C) and with use of the miScript RT Kit. The thus produced cDNA was tested in a real-time PCR to detect GAPDH.

FIG. 22 shows various amounts (1-100 ng) of miRNeasy RNA, which were reverse transcribed with use of miScript in the presence or absence of various amounts of poly-(C). The thus produced cDNA was used in a real-time PCR, in this case to test CDC2.

FIG. 23 shows the use of 1 ng of miRNeasy RNA, which was reverse transcribed in the presence or absence of 50 ng of poly-(C) and with use of the miScript RT Kit. The thus produced cDNA was tested in a real-time PCR to detect CDC2. 

What is claimed is:
 1. A reaction mixture comprising: a. RNA; b. a first enzyme with polyadenylation activity, c. a second enzyme with reverse transcriptase activity; d. a buffer; e. at least one ribonucleotide; f. at least one deoxyribonucleotide comprising: i. a modification selected from the group consisting of a biotinylation, a digoxigenin, and a hapten; or ii. a label selected from the group consisting of a radioactive label and a fluorescent label; and g. an anchor olignucleotide comprising a poly(T) sequence capable of being extended to form cDNA using the RNA as a template.
 2. The reaction mixture of claim 1, wherein the RNA is selected from the group consisting of prokaryotic RNA, eukaryotic RNA, viral RNA, archae RNA, miRNA, snoRNA, mRNA, tRNA, non-polyadenylated RNA, rRNA and mixtures thereof.
 3. The reaction mixture of claim 1, wherein the anchor oligonucleotide comprises a 5′-tail sequence.
 4. The reaction mixture of claim 3, wherein the anchor oligonucleotide has a length of between 6 and 150 nucleotides, and optionally comprises an anchor sequence on the 3′-end.
 5. The reaction mixture of claim 4, wherein the anchor oligonucleotide is selected from the group consisting of a deoxyribonucleic acid (DNA), a peptide-nucleic acid (PNA), a locked nucleic acid (LNA), a phosphorus thioate-deoxyribonucleic acid, a cyclohexene-nucleic acid (CeNA), an N3′-P5′-phosphorus amidate (NP) and a tricyclo-deoxyribonucleic acid (tcDNA).
 6. The reaction mixture of claim 1, wherein the at least one ribonucleotide is selected from the group consisting of adenosine-5′-triphosphate, and adenosine-5′-triphosphate with a base analog, wherein the ribonucleotide is optionally modified or labeled.
 7. The reaction mixture of claim 1, wherein the deoxyribonucleotide is selected from the group consisting of deoxyadenosine-5′-triphosphate (dATP), deoxythymine-5′-triphosphate (dTTP), deoxycytosine-5′-triphosphate (dCTP), deoxyguamine-5′-triphosphate (dGTP), and deoxyuracil-5′-triphosphate (dUTP).
 8. The reaction mixture of claim 1, wherein the radioactive label is selected from the group consisting of ³²P, ³³P, ³⁵S, and ³H.
 9. The reaction mixture of claim 1, wherein the fluorescent label is selected from the group consisting of fluorescein isothiocyanate (FITC), 6-carboxyfluorescein (FAM), xanthene, rhodamine, 6-carboxy-2′,4′,7′,4,7-hexachlorofluorescein, 6-carboxy-4′,5′-dichloro-2′,7′-dimethoxy fluorescein, N,N,N′,N′-tetramethyl-6-carboxyrhodamine, 6-carboxy-X-rhodamine, 5-carboxyrhodamine-6G, 6-carboxyrhodamine-6G, rhodamine 110, coumarins, umbelliferones, benzimides, phenanthridines, ethidium bromides, acridine dyes, carbazole dyes, phenoxazine dyes, porphyrine dyes, polymethine dyes; cyanine dyes, Cy3, Cy5, Cy7, quinoline dyes and alexa dyes.
 10. The reaction mixture of claim 1, wherein the concentration of the deoxyribonucleotide is at least 0.01 mmol in the reaction mixture and at most 10 mmol in the reaction mixture.
 11. The reaction mixture of claim 10, wherein the concentration of the deoxyribonucleotide is at least 0.2 mmol to at most 2 mmol.
 12. The reaction mixture of claim 1, wherein the buffer has a pH of 6 to 10 and comprises Mg2+ ions.
 13. The reaction mixture of claim 1, wherein the enzyme with polyadenylation activity is selected from the group consisting of an enzyme of prokaryotic origin, an enzyme of eukaryotic origin, an enzyme of viral origin, an enzyme of archae origin and an enzyme of plant origin.
 14. The reaction mixture of claim 13, wherein the enzyme with polyadenylation activity is selected from the group consisting of a poly(A)-polymerase from Escherichia coli, a poly(A)-polymerase from yeast, a poly(A)-polymerase from cattle, a poly(A)-polymerase from frogs, and a human poly(A)-polymerase.
 15. The reaction mixture of claim 1, wherein the enzyme with reverse transcriptase activity is selected from the group consisting of an enzyme from a virus, an enzyme from a bacteria, an enzyme from an archae bacteria, an enzyme from a eukaryote and an enzymes from a thermostable organism.
 16. The reaction mixture of claim 15, wherein the enzyme with reverse transcriptase activity is selected from the group consisting of HIV Reverse Transcriptase, M-MLV Reverse Transcriptase, EAIV Reverse Transcriptase, AMV Reverse Transcriptase, Thermus thermophilus DNA polymerase 1, and M-MLV RNAse H.
 17. The reaction mixture of claim 1, further comprising a thermostable enzyme with DNA-synthesis activity, and at least one oligonucleotide for specific detection of cDNA. 